1,363 results match your criteria Cystic Hygroma Imaging


Retroperitoneal mesothelial cyst misdiagnosed as a congenital choledochal cyst for an infant patient: A case report and literature review.

Int J Surg Case Rep 2020 May 8;71:176-178. Epub 2020 May 8.

Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, Sichuan Province, People's Republic of China.

Introduction: Mesothelial cyst (MC) is very uncommon in clinic, which could occasionally occur in peritoneal, retroperitoneal or even pleural cavity.

Presentation Of Case: We hereby described an infant patient with retroperitoneal MC who was misdiagnosed as congenital choledochal cyst by both radiologists and clinicians. A choledochal cyst resection with hepatojejunostomy under the da Vinci surgical system was routinely prepared for this patient but a local resection for the whole lesion was unexpectedly performed during the operation. Read More

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http://dx.doi.org/10.1016/j.ijscr.2020.04.075DOI Listing

Intra-abdominal cystic lymphangioma of the mesocolon sigmoids: a rare entity in adult patient woman.

J Surg Case Rep 2020 May 15;2020(5):rjaa031. Epub 2020 May 15.

Medico, Ministerio de Salud Publica, Quito, Ecuador.

The lymphangioma is a benign neoplasm, mostly connate, it occurs more often in children. It is more frequently located in the head-neck region, as well as in the armpit, and less frequently in the abdomen. The diagnosis, as well as their appearance is variant, they can be asymptomatic depending on the size. Read More

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http://dx.doi.org/10.1093/jscr/rjaa031DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229823PMC

Bronchogenic cyst of the stomach: A case report.

World J Clin Cases 2020 Apr;8(8):1525-1531

Department of Endoscopy, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, and Tianjin's Clinical Research Center for Cancer, Tianjin 300060, China.

Background: Gastric bronchogenic cysts (BCs) are extremely rare cystic masses caused by abnormal development of the respiratory system during the embryonic period. Gastric bronchial cysts are rare lesions first reported in 1956; as of 2019, only 37 cases are available in the MEDLINE/PubMed online databases. BCs usually have no clinical symptoms in the early stage, and their imaging findings also lack specificity. Read More

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http://dx.doi.org/10.12998/wjcc.v8.i8.1525DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190944PMC

Cystic lymphangioma of breast: a rare presentation.

BMJ Case Rep 2020 Apr 26;13(4). Epub 2020 Apr 26.

Radiodiagnosis, SGPGIMS, Lucknow, Uttar Pradesh, India

A 36-year-old woman presented to the radiology department with a history of gradual increase in the size of her left breast and greenish discolouration of the skin over it since 1.5 months. Physical examination revealed a soft non-tender mass involving the whole of the left breast. Read More

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http://dx.doi.org/10.1136/bcr-2020-235040DOI Listing

Imaging features, complications and differential diagnoses of abdominal cystic lymphangiomas.

Abdom Radiol (NY) 2020 Apr 15. Epub 2020 Apr 15.

Department of Digestive Diagnostic and Interventional Radiology, University Hospital Claude Huriez - Regional University Hospital Center, rue Michel Polonoski, 59037, Lille Cedex, France.

Purpose: The aim of the study is to describe the imaging features, complications and differential diagnoses of abdominal cystic lymphangiomas (ACLs).

Results: ACLs are benign lymphatic malformations that mainly arise in the subperitoneal space and the retroperitoneum. The typical presentation of an ACL is a multilocular lesion with homogenous serous content, presenting a thin wall and septa, usually free from adjacent organ compression. Read More

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http://dx.doi.org/10.1007/s00261-020-02525-3DOI Listing

Non-adrenal tumors of the adrenal area; what are the pitfalls?

J Visc Surg 2020 Mar 19. Epub 2020 Mar 19.

Clinique de chirurgie digestive et endocrinienne, institut des maladies de l'appareil digestif, centre hospitalier universitaire de Nantes, 44093 Nantes, France. Electronic address:

Discovery of an adrenal mass is nowadays a frequent situation. While adrenal tumors can cause a variety of symptoms, more often than not they are diagnosed incidentally on imaging exams such as CT-scan or MRI performed for another purpose. However, any retroperitoneal supra-renal mass can have an extra-adrenal origin. Read More

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http://dx.doi.org/10.1016/j.jviscsurg.2020.02.004DOI Listing

Giant Cystic Mediastinal Lymphangioma.

Eur J Case Rep Intern Med 2020 24;7(1):001323. Epub 2019 Dec 24.

Internal Medicine Department, Centro Hospitalar Universitário Cova da Beira, Covilhã, Portugal.

Cystic lymphangioma mainly occurs in children and develops from the lymphatic vessels. The present study reports the case of a 36-year-old female patient with a giant cystic mediastinal lymphangioma. She was asymptomatic and the diagnosis was accidental. Read More

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http://dx.doi.org/10.12890/2019_001323DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993911PMC
December 2019

Splenic mass of uncertain etiology in a 15-year-old male patient: a case report.

Acute Med Surg 2020 Jan-Dec;7(1):e464. Epub 2019 Oct 28.

Department of Emergency Medicine Saitama Medical Center Saitama Medical University Saitama Japan.

Background: There are few reports on spleen masses, and solitary splenic abscesses with abdominal pain have not been reported in younger age groups. We report a case of a splenic mass of uncertain etiology in a 15-year-old boy.

Case Presentation: A 15-year-old boy visited the emergency department with abdominal pain. Read More

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http://dx.doi.org/10.1002/ams2.464DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971432PMC
October 2019

Congenital cervical choristoma of the neck mimicking cystic lymphangioma.

Eur Ann Otorhinolaryngol Head Neck Dis 2020 Jan 23. Epub 2020 Jan 23.

Faculté de médecine et de pharmacie de Rabat, Université Mohammed V Rabat, Rabat, Morocco; Service d'anatomie pathologique, l'hôpital des Spécialités de Rabat, CHU de Rabat, Rabat, Morocco.

Introduction: Choristoma is a mass presenting normal histology, but in an abnormal location. Cystic choristoma is rarely reported in the head and neck region. Neonatal cystic masses in the neck suggest usually correspond to a diagnosis of cystic lymphangioma. Read More

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http://dx.doi.org/10.1016/j.anorl.2020.01.009DOI Listing
January 2020

[CASE REPORT: COMPLETE RESECTION OF RETROPERITONEAL CYSTIC LYMPHANGIOMA AND SURROUNDING ORGANS].

Nihon Hinyokika Gakkai Zasshi 2019 ;110(1):52-55

Department of Urology, Nippon Medical School Hospital.

A 65-year-old man was admitted to our institution with vomiting and right flank pain. Computed tomography (CT) imaging showed a 21-cm retroperitoneal multilocular cystic tumor which had been identified four years previously. It had increased from 17 to 21 cm. Read More

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http://dx.doi.org/10.5980/jpnjurol.110.52DOI Listing
January 2019

Laparoscopic resection of abdominal cystic lymphangioma derived from lesser omentum: Case report.

Medicine (Baltimore) 2020 Jan;99(1):e18641

Rationale: Cystic lymphangiomas are uncommon congenital malformations that originate from lymphatic channels. Lymphangiomas frequently appear in the head, neck, and axillary regions of children. Abdominal cystic lymphangiomas are extremely rare, having a reported incidence of 1 in 20,000 to 250,000. Read More

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http://dx.doi.org/10.1097/MD.0000000000018641DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946562PMC
January 2020

Diagnosis of Pancreatic Cystic Lesions by Virtual Slicing: Comparison of Diagnostic Potential of Needle-Based Confocal Laser Endomicroscopy versus Endoscopic Ultrasound-Guided Fine-Needle Aspiration.

J Pathol Inform 2019 13;10:34. Epub 2019 Nov 13.

Department of Pathology, The Institute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York City, New York, USA.

Background: Pancreatic cystic lesions are often challenging entities for diagnosis and management. EUS-FNA diagnostic accuracy is limited by paucicellularity of cytology specimens and sampling errors. Needle-based confocal laser endomicroscopy (nCLE) provides real-time imaging of the microscopic structure of the cystic lesion and could result in a more accurate diagnosis. Read More

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http://dx.doi.org/10.4103/jpi.jpi_32_19DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883479PMC
November 2019

Generalized cystic lymphangiomatosis incidentally recognized in an asymptomatic adult: Peroperative, CT, MRI, and histopathological findings of a very rare case.

Niger J Clin Pract 2019 Dec;22(12):1778-1780

Department of Gastrointestinal Surgery, ZTB Women's Health Research and Education Hospital, Ankara, Turkey.

Generalized cystic lymphangiomatosis is an uncommon congenital lymphatic malformation that may affect soft and hard tissues as well as organs. It is rarely seen in adult patients. Osseous lesions appear as well-defined cystic lesions with a sclerotic rim without periosteal reaction or a soft tissue component. Read More

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http://dx.doi.org/10.4103/njcp.njcp_582_18DOI Listing
December 2019

Case report: horse or zebra, ascites or pseudo-ascites? Care for pictural details!

BMC Pediatr 2019 11 25;19(1):460. Epub 2019 Nov 25.

Department of Translational Medical Science, Section of Pediatrics, University of Naples Federico II, Via Sergio Pansini n. 5, 80131, Naples, Italy.

Background: Pseudo-ascites is a very rare condition in children and remains a challenging diagnosis. Targeted imaging may be helpful, but a high index of clinical suspicion is often necessary to guide the investigations, as pseudo-ascites may efficiently mimic true ascites. To date, still many cases of pseudo-ascites suffer diagnostic and therapeutic delay, and some are only diagnosed during surgical exploration. Read More

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http://dx.doi.org/10.1186/s12887-019-1826-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6876094PMC
November 2019

Preoperative contrast-enhanced computed tomographic characterisation of pancreatic cystic lesions: A prospective study.

SA J Radiol 2019 10;23(1):1727. Epub 2019 Jun 10.

Department of Radiodiagnosis, Sher-I-Kashmir Institute of Medical Sciences, Srinagar, India.

Background: Characterisation of pancreatic cystic lesions has a direct role in their management and computed tomography is the mainstay of investigation for diagnosing and characterising them.

Objectives: The aim of this study was to prospectively assess the diagnostic accuracy of contrast-enhanced computed tomography (CECT) in preoperative characterisation of pancreatic cystic lesions with histopathology as the reference standard.

Method: A total of 38 patients with cystic pancreatic lesions diagnosed after clinical, laboratory and sonographic evaluation, irrespective of age, were preoperatively evaluated with CECT. Read More

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http://dx.doi.org/10.4102/sajr.v23i1.1727DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837796PMC

Cystic lymphangioma in the peripheral jejunal mesentery in an adult and excision with laparoscopic-assisted surgery: a case report.

World J Surg Oncol 2019 Oct 24;17(1):170. Epub 2019 Oct 24.

Department of Human Pathology Kanazawa University Graduate School of Medicine, 13-1, Takara-machi, Kanazawa, Ishikawa, 920-8640, Japan.

Background: Lymphangiomas are uncommon congenital malformations that present mainly in the head, neck, and axillar regions in pediatric patients. Mesenteric cystic lymphangiomas (MCLs), which occasionally present with substantial growth and the invasion of adjacent vital structures, are rarely reported in adults. We report a case of MCL in an adult who was treated with laparoscopic-assisted excision. Read More

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http://dx.doi.org/10.1186/s12957-019-1713-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814111PMC
October 2019
1 Read

Cavernous Lymphangioma in the Maxillary Sinus.

J Craniofac Surg 2019 Nov-Dec;30(8):2520-2521

Department of Otolaryngology-Head and Neck Surgery, Chonnam National University Medical School & Chonnam National University Hwasun Hospital, Jeonnam, South Korea.

Lymphangioma in the maxillary sinus is rare. Herein, the authors report an unusual case of cavernous lymphangioma, in the maxillary sinus, with imaging examinations. Clinicians should be aware of the possibility of lymphangioma in the maxillary sinus, and be capable of distinguishing it, from other benign cystic lesions. Read More

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http://dx.doi.org/10.1097/SCS.0000000000006003DOI Listing
January 2020
4 Reads
0.676 Impact Factor

Role of Ultrasound in Emergency Front of Neck Access: A Case Report and Review of Literature.

A A Pract 2019 Nov;13(10):382-385

From the University Hospitals Coventry and Warwickshire NHS Trust, Coventry, United Kingdom.

Emergency front of neck access (eFONA) is a lifesaving procedure in a cannot intubate cannot oxygenate (CICO) situation. We report a case of a patient who presented to the emergency department (ED) in extremis with a difficult airway. A history of multiple neck surgeries and permanent tracheostomy from birth until the age of 17 years complicated his airway management. Read More

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http://dx.doi.org/10.1213/XAA.0000000000001089DOI Listing
November 2019
1 Read

Large cystic lymphangioma of pancreas mimicking mucinous neoplasm: case report with a review of histological differential diagnosis.

Int Med Case Rep J 2019 3;12:297-301. Epub 2019 Sep 3.

Shiraz Transplant Center, Abu Ali Sina Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.

Purpose: Cystic lymphangioma of the pancreas was first recognized in 1913 as a form of benign cyst. It is extremely rare, accounting for less than 1% of the lymphangiomas.

Case Report: Herein, we report a case of cystic pancreatic lymphangioma diagnosed in a 51-year-old female patient who was hospitalized for a colicky upper abdominal pain for a month. Read More

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http://dx.doi.org/10.2147/IMCRJ.S218056DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731960PMC
September 2019
4 Reads

Magnetic resonance imaging of adrenal gland: state of the art.

Gland Surg 2019 Sep;8(Suppl 3):S223-S232

Department of Medicine and Surgery, Unit of Radiologic Science, University of Parma, Maggiore Hospital, Parma, Italy.

Detection of adrenal lesions, because of the widespread use of imaging and especially high-resolution imaging procedures, is increased. Because of the importance to characterize those findings, magnetic resonance imaging (MRI), in particular chemical shift imaging (CSI), is useful to distinguish whether a lesion is benignant or malignant and to avoid further diagnostic or surgical procedures. It represents the first choice of imaging in patient like children or pregnant women, and a valid complement to other imaging techniques like CT or PET/CT. Read More

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http://dx.doi.org/10.21037/gs.2019.06.02DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6755942PMC
September 2019
3 Reads

Cystic Lesions of the Pancreas: Differential Diagnosis and Cytologic-Histologic Correlation.

Arch Pathol Lab Med 2020 01 20;144(1):47-61. Epub 2019 Sep 20.

From the Department of Pathology, Medical College of Wisconsin, Milwaukee (Drs Abdelkader, Hunt, Hartley, and Giorgadze); and the Department of Pathology, Albert Einstein College of Medicine, The Bronx, New York (Dr Panarelli).

Context.—: Pancreatic cystic lesions (PCLs) are very common, and their detection is increasing with the advances in imaging techniques. Because of the major implications for management, distinguishing between neoplastic and nonneoplastic PCLs is critical. Read More

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http://dx.doi.org/10.5858/arpa.2019-0308-RADOI Listing
January 2020
5 Reads

Update on MR Imaging of cystic retroperitoneal masses.

Abdom Radiol (NY) 2019 Sep 9. Epub 2019 Sep 9.

The Ottawa Hospital, The University of Ottawa, 1053 Carling Avenue, Ottawa, ON, K1Y 4E9, Canada.

Objective: This article reviews the MRI appearance of cystic retroperitoneal (RP) masses.

Conclusion: Lymphangiomas are the most common RP cystic masses and typically appear simple; microscopic fat is a specific but insensitive finding. Location, internal complexity, and enhancement pattern suggest alternative diagnoses which range from normal anatomic variants to congenital abnormalities and importantly include benign, neurogenic, and malignant neoplasms. Read More

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http://dx.doi.org/10.1007/s00261-019-02196-9DOI Listing
September 2019
5 Reads

Rare case of cystic hygroma in the epidural space resulting in multilevel spinal cord compression.

BMJ Case Rep 2019 Aug 28;12(8). Epub 2019 Aug 28.

Allegheny General Hospital - Western Pennsylvania Hospital Medical Education Consortium, Pittsburgh, Pennsylvania, USA.

Lymphangioma, or cystic hygroma, involving the epidural space and spinal soft tissue, is a rare benign lesion consisting of an abnormal collection of lymphatic tissue isolated from the normal lymphatic system. This case report is the most extensive case of cystic hygroma involving the spine reported in the literature. A 23-year-old man with a history of cystic hygromas of the neck and thorax presented with bilateral upper and lower extremity weakness that progressively worsened over 3 months. Read More

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http://dx.doi.org/10.1136/bcr-2019-230326DOI Listing
August 2019
2 Reads

Large intra-abdominal cystic lymphangioma managed by laparoscopic partial excision and modified drain with no need for open resection.

BMJ Case Rep 2019 Aug 21;12(8). Epub 2019 Aug 21.

Department of Surgery, Cairns Hospital, Cairns North, Queensland, Australia.

A 57-year-old woman was referred to the emergency department after a CT scan ordered by her general practitioner to investigate her abdominal pain showed a large cystic mass. The simple cystic appearance with its location in the small bowel mesentery prompted a provisional diagnosis of cystic lymphangioma. However, concerns regarding the size, location and local involvement of neurovascular structures presented a technical surgical challenge. Read More

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http://dx.doi.org/10.1136/bcr-2019-229227DOI Listing
August 2019
2 Reads

Gastric duplication cyst mimicking large cystic lymphangioma in an adult: A rare case report and review of the literature.

World J Clin Cases 2019 Aug;7(15):2087-2093

Department of Radiology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou 310000, Zhejiang Province, China.

Background: Gastric duplication cysts (GDCs) are a relatively uncommon congenital developmental abnormality, mainly occurring in infants but very rarely in adults. Because of the variability in clinical presentation, it is often quite challenging to diagnose GDCs in adults. We are presenting a case report of an adult diagnosed operatively as having a GDC with a literature review to summarize clinical and imaging features and the treatment selections of GDCs in adults so that doctors could have a comprehensive understanding of this disease and make a precise diagnosis and a suitable therapeutic decision for patients. Read More

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http://dx.doi.org/10.12998/wjcc.v7.i15.2087DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695537PMC
August 2019
2 Reads

Fetal giant right cervical cyst causing severe tracheal compression: A case report.

Medicine (Baltimore) 2019 Aug;98(31):e16670

Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education.

Rationale: Fetal giant cervical cyst (FGCC) is a rare congenital anomaly. Sometimes FGCC may extend into the mediastinum, and result in severe tracheal compression, which is a life-threatening event at birth.

Patient Concerns: We present a rare case of FGCC, which extended from the right neck into the superior mediastinum, and resulted in severe tracheal compression. Read More

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http://dx.doi.org/10.1097/MD.0000000000016670DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709085PMC
August 2019
8 Reads

Antenatal diagnosis of cardio-facio-cutaneous syndrome: Prenatal characteristics and contribution of fetal facial dysmorphic signs in utero. About a case and review of literature.

Eur J Obstet Gynecol Reprod Biol 2019 Sep 16;240:232-241. Epub 2019 Jul 16.

Center for Human Genetics, Saint-Luc University Hospital, UCL, Brussels, Belgium.

Antenatal diagnosis of cardio-facio-cutaneous syndrome: prenatal characteristics and contribution of fetal facial dysmorphic signs in utero. This paper is a case study and review of literature. "RASopathies" is the term coined for a group of genetic diseases that share modulation inside the MAPKinase pathway. Read More

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http://dx.doi.org/10.1016/j.ejogrb.2019.06.035DOI Listing
September 2019
7 Reads

A case report of Turner syndrome associated with fetal nuchal cystic hygroma and bilateral syndactyly of the hands and feet.

Ital J Pediatr 2019 Jul 18;45(1):85. Epub 2019 Jul 18.

Department of Obstetrics and Gynecology, Wenzhou People's Hospital, Wenzhou Maternal and Child Health Care Hospital, The Third Clinical Institute Affiliated To Wenzhou Medical University, Wenzhou, 325000, China.

Background: Turner syndrome (45,X), accounts for 1-2% of conceptions which typically miscarry early in the first trimester. Cases detected prenatally often present with cystic hygroma, which is an ultrasound marker for aneuploidy generally, but Turner syndrome particularly. In this study, we report a second trimester intrauterine fetal demise (IUFD), complicated by a marked cystic hygroma and bilateral syndactyly of the fingers and toes. Read More

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http://dx.doi.org/10.1186/s13052-019-0680-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639934PMC
July 2019
10 Reads

Are Hygromas and Hydrocephalus After Decompressive Craniectomy Caused by Impaired Brain Pulsatility, Cerebrospinal Fluid Hydrodynamics, and Glymphatic Drainage? Literature Overview and Illustrative Cases.

World Neurosurg 2019 Oct 11;130:e941-e952. Epub 2019 Jul 11.

Department of Neurosurgery, The Permanente Medical Group, Kaiser Sacramento Medical Center, Sacramento, California, USA.

Background: Poorly understood cranial fluid accumulations are frequently observed after decompressive craniectomy and often termed "external hydrocephalus." These findings are difficult to explain using traditional models of hydrocephalus.

Methods: Representative cases, clinical management, and literature overview are presented. Read More

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http://dx.doi.org/10.1016/j.wneu.2019.07.041DOI Listing
October 2019
1 Read

Αdnexal cystic lymphangiomas in patients with massive leiomyomatous uterus: a not so uncommon finding on pelvic MRI.

Abdom Radiol (NY) 2020 02;45(2):537-546

Department of Radiology, School of Medicine, Aretaieion Hospital, National and Kapodistrian University of Athens, 76 Vassilisis Sofias Ave, Athens, 11528, Greece.

Purpose: To investigate any association between the presence of an adnexal cystic lymphangioma (ACL) and an enlarged leiomyomatous uterus.

Methods: A retrospective observational study was conducted by two expert radiologists using a 10-year MRI database (2008-2018); 85 patients (mean age: 45.5 years ± 10. Read More

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http://dx.doi.org/10.1007/s00261-019-02106-zDOI Listing
February 2020
9 Reads

Pleural-Based Intrathoracic Cystic Lymphangioma in an Infant Mimicking a Pneumonia.

Case Rep Pediatr 2019 6;2019:7920591. Epub 2019 May 6.

Pediatric Pulmonary Unit, Shaare Zedek Medical Center, Affiliated to the Hebrew University, School of Medicine, Jerusalem, Israel.

Cystic lymphangioma is an uncommon benign tumor that occurs primarily in children in the cervical region. We report the first case of a pleural-based cystic lymphangioma in an infant. The patient was admitted for RUL pneumonia. Read More

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http://dx.doi.org/10.1155/2019/7920591DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6526578PMC
May 2019
9 Reads

Management of a case of orbital lymphangioma presenting in adulthood with negative-pressure aspiration and bleomycin injection.

BMJ Case Rep 2019 Jun 8;12(6). Epub 2019 Jun 8.

Department of Ophthalmology, All India Institute of Medical Sciences, New Delhi, India.

We hereby report a case of a 55-year-old woman, with complaints of sudden onset outward protrusion of left eye progressing over 2 months, along with pain and loss of vision. Visual acuity in the affected eye was light perception only. On imaging, a well-defined solitary cystic lesion was noted in the retrobulbar space, which showed no enhancement on contrast-enhanced MRI. Read More

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http://dx.doi.org/10.1136/bcr-2018-227697DOI Listing
June 2019
10 Reads

Primary Supraclavicular Cystic Lymphangioma in an Adult: A Rare Presentation.

J Coll Physicians Surg Pak 2019 Jun;29(6):S11-S12

Department of General Surgery, Combined Military Hospital (CMH), Rawalpindi, Pakistan.

Cervicothoracic cystic lymphangiomas are found commonly in children less than 2 years of age, but the same are rare in adults. These form as a result of abberant development of embryonic lymph sac which is gradually filled with lymph fluid.1 They are commonly found in the head and neck region but can be present anywhere in the body. Read More

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http://dx.doi.org/10.29271/jcpsp.2019.06.S11DOI Listing
June 2019
16 Reads

Cystic hygroma and micromelic lower limbs: First-trimester sonographic markers of campomelic dysplasia.

Eur J Obstet Gynecol Reprod Biol 2019 Jul 21;238:191-193. Epub 2019 May 21.

Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center Affiliated to Guangzhou Medical University, Guangzhou, China. Electronic address:

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http://dx.doi.org/10.1016/j.ejogrb.2019.05.021DOI Listing
July 2019
1 Read

Cystic lymphangioma of the breast.

Breast J 2019 05 10;25(3):523-525. Epub 2019 Apr 10.

Department of Radiology, Complexo Hospitalario Universitario A Coruña, La Coruña, Spain.

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http://dx.doi.org/10.1111/tbj.13269DOI Listing
May 2019
6 Reads

A case report of complicated appendicular hydatid cyst mimicking an appendiceal mucocele.

Clin J Gastroenterol 2019 Dec 10;12(6):574-577. Epub 2019 Apr 10.

Department B of Surgery, Charles Nicolle Hospital, Tunis, Tunisia.

Retaining the etiology of a cystic lesion in the right iliac fossa can be difficult. Appendicular hydatid cyst is a very uncommon cause of a such lesion. In some cases, diagnosis is not obvious. Read More

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http://dx.doi.org/10.1007/s12328-019-00981-zDOI Listing
December 2019
5 Reads

Cystic lesion of pectoralis minor muscle: learning from mistakes.

Autops Case Rep 2019 Apr-Jun;9(2):e20180780. Epub 2019 Mar 22.

Miguel Servet University Hospital, Department of Pathology. Zaragoza, Spain.

Hydatidosis is a frequent infestation in large endemic areas, caused by helminths. Primary localization within the muscle or bone tissues is rare. We report the case of a 52-year-old woman with a cystic lesion located in the right pectoralis minor muscle, who was initially diagnosed with cystic lymphangioma by imaging examination. Read More

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http://dx.doi.org/10.4322/acr.2018.078DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433142PMC
March 2019
14 Reads

Prenatal ultrasound diagnosis of fetal chest wall cystic lymphangioma: An Italian case series.

Eur J Obstet Gynecol Reprod Biol 2019 May 18;236:139-142. Epub 2019 Mar 18.

Department of Neuroscience, Reproductive Sciences and Dentistry, School of Medicine, University of Naples Federico II, Naples, Italy; Diagnosi Ecografica e Prenatale di A.Di Meglio, Naples, Italy.

Fetal lymphangioma is a rare congenital malformation of lymphatic system that involve the skin and the subcutaneous tissue. The vast majority of the lymphangioma occurs in the neck. More rarely lymphangiomas may occur in the axillary region, including chest wall. Read More

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http://dx.doi.org/10.1016/j.ejogrb.2019.03.014DOI Listing
May 2019
9 Reads
1.627 Impact Factor

What did I just aspirate? Rare pancreatic cyst.

Gastrointest Endosc 2019 07 15;90(1):164-165. Epub 2019 Mar 15.

Division of Gastroenterology and Hepatology, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

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https://linkinghub.elsevier.com/retrieve/pii/S00165107193016
Publisher Site
http://dx.doi.org/10.1016/j.gie.2019.03.004DOI Listing
July 2019
11 Reads

Cystic lymphangiomatous lesions of the adrenal gland: A clinicopathological study of 37 cases including previously unreported cysts with papillary endothelial proliferation.

Pathol Res Pract 2019 Jun 6;215(6):152385. Epub 2019 Mar 6.

Department of Pathology, Medical University of Warsaw, ul. Pawińskiego 7, 02-142, Warsaw, Poland.

Published data regarding lymphangiomatous cysts of the adrenal glands (also known as adrenal cystic lymphangiomas) are limited to case reports and a few small case series. We analyzed the clinicopathologic features and histomorphologic spectrum of 37 cases of adrenal cystic lymphangiomatous lesions. There were 26 females and 11 males ranging from 12 to 67 years old (median, 34 years). Read More

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https://linkinghub.elsevier.com/retrieve/pii/S03440338183182
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http://dx.doi.org/10.1016/j.prp.2019.03.014DOI Listing
June 2019
8 Reads

Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.

Nat Med 2019 03 28;25(3):439-447. Epub 2019 Jan 28.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

Current non-invasive prenatal screening is targeted toward the detection of chromosomal abnormalities in the fetus. However, screening for many dominant monogenic disorders associated with de novo mutations is not available, despite their relatively high incidence. Here we report on the development and validation of, and early clinical experience with, a new approach for non-invasive prenatal sequencing for a panel of causative genes for frequent dominant monogenic diseases. Read More

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http://www.nature.com/articles/s41591-018-0334-x
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http://dx.doi.org/10.1038/s41591-018-0334-xDOI Listing
March 2019
48 Reads

Mammary Analogue Secretory Carcinoma Arising in the Parotid Gland of Child.

Plast Reconstr Surg Glob Open 2018 Dec 13;6(12):e2059. Epub 2018 Dec 13.

Department of Plastic and Reconstructive Surgery, Juntendo University School of Medicine, Tokyo, Japan.

Mammary analogue secretory carcinoma (MASC) of salivary glands is a newly recognized tumor entity. We report a child who was initially diagnosed with lymphangioma and referred to our institute for sclerotherapy, only to find out that the tumor was in fact MASC after excision. This case of MASC is in a 7-year-old boy, the youngest case so far reported. Read More

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http://dx.doi.org/10.1097/GOX.0000000000002059DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326613PMC
December 2018
8 Reads

Giant intra-abdominal cystic lymphangioma.

Korean J Intern Med 2019 May 7;34(3):678-679. Epub 2019 Jan 7.

Department of Pathology, Sakarya University Research and Educational Hospital, Sakarya, Turkey.

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http://dx.doi.org/10.3904/kjim.2017.029DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506744PMC
May 2019
2 Reads

Adult-onset giant cervical cystic hygroma with pressure manifestations on aerodigestive tract, managed surgically: reporting of a rare case.

Ann R Coll Surg Engl 2019 Mar 3;101(3):e84-e87. Epub 2019 Jan 3.

Department of General Surgery, King Fahd Central Hospital , Jazan , Saudi Arabia.

Cystic hygroma is a benign congenital malformation of the lymphatic system that occurs in children younger than two years of age. Hygroma commonly presents in head and neck but can be present anywhere. It is rarely seen in adults. Read More

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http://dx.doi.org/10.1308/rcsann.2018.0214DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400928PMC
March 2019
8 Reads

Cystic lymphangioma of the pancreas: a hard diagnostic challenge between pancreatic cystic lesions-review of recent literature.

Gland Surg 2018 Oct;7(5):487-492

Department of Human Pathology of the Adult and Evolutive Age "Gaetano Barresi", Section of General Surgery, University of Messina, Messina, Italy.

Lymphangiomas are rare congenital benign tumors arising from the lymphatic system. The incidence of this disease in the pancreas is extremely rare, accounting for less than 1% of these tumors. Before introducing the review we reported a case of a 67-year-old woman with cystic lymphangioma of the pancreas. Read More

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http://gs.amegroups.com/article/view/19144/21358
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http://dx.doi.org/10.21037/gs.2018.04.02DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6234244PMC
October 2018
48 Reads

Cystic Hygroma: A Preliminary Genetic Study and a Short Review from the Literature.

Lymphat Res Biol 2019 Feb 22;17(1):30-39. Epub 2018 Nov 22.

2 Magi's Lab, Rovereto, Italy.

Background: The objective of this study is to examine the hypothesis that cystic hygroma (CH) with normal karyotype can manifest as a Mendelian inherited trait, and that a genetic similitude with hereditary lymphedema exists. To reach this goal, we investigated the prevalence of genetic variants in angiogenesis and lymphangiogenesis genes in a cohort of euploid fetuses with CH that almost resolved before delivery. A short review of cases from literature is also reported. Read More

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https://www.liebertpub.com/doi/10.1089/lrb.2017.0084
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http://dx.doi.org/10.1089/lrb.2017.0084DOI Listing
February 2019
31 Reads

[Left-sided Chylothorax and Tumor of the Right Anterior Mediastinum].

Pneumologie 2018 Dec 19;72(12):851-854. Epub 2018 Nov 19.

Thoraxchirurgische Abteilung des LungenZentrums Saar, SHG-Kliniken, Völklingen.

An 82-year-old male patient presented with a left-sided spontaneous chylothorax. A computed tomographic scan of the chest revealed a cystic tumor in the right upper anterior mediastinum and nodules in the left mediastinum that we interpreted as enlarged lymph nodes. On suspicion of lymphoma and for therapy of chylothorax, we performed a left-sided thoracotomy. Read More

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http://www.thieme-connect.de/DOI/DOI?10.1055/a-0767-7882
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http://dx.doi.org/10.1055/a-0767-7882DOI Listing
December 2018
41 Reads

Pancreatic Lymphangioma: A Case Report and Literature Review.

J Comput Assist Tomogr 2019 Mar/Apr;43(2):242-244

Department of Radiology, Thomas Jefferson University School of Medicine, Philadelphia, PA.

We report a case of a 29-year-old woman with a pancreatic lymphangioma who presented clinically as a case of acute pancreatitis. Lymphangiomas are benign tumors of vascular origin with lymphatic differentiation, most commonly found in the head and neck. Pancreatic lymphangiomas are extremely rare, accounting for only 1% of abdominal lymphangiomas, with approximately 60 cases reported in the literature. Read More

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http://dx.doi.org/10.1097/RCT.0000000000000818DOI Listing
April 2019
29 Reads

First-trimester cystic hygroma and omphalocele in a fetus with Turner syndrome.

Taiwan J Obstet Gynecol 2018 Oct;57(5):763-764

Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan; Department of Bioengineering, Tatung University, Taipei, Taiwan.

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https://linkinghub.elsevier.com/retrieve/pii/S10284559183019
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http://dx.doi.org/10.1016/j.tjog.2018.08.030DOI Listing
October 2018
36 Reads

Intra-Abdominal Cystic Lymphangioma.

J Pediatr 2019 Feb 11;205:288-288.e1. Epub 2018 Oct 11.

Womens and Perinatal Services Leicester Royal Infirmary University Hospitals of Leicester Leicester, United Kingdom.

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http://dx.doi.org/10.1016/j.jpeds.2018.09.034DOI Listing
February 2019
9 Reads