Search our Database of Scientific Publications and Authors

I’m looking for a

    6464 results match your criteria Benign Lymphangioendothelioma

    1 OF 130

    An acute presentation of pediatric mesenteric lymphangioma: a case report and literature overview.
    Acta Chir Belg 2017 Sep 19:1-5. Epub 2017 Sep 19.
    a Departments of General Surgery , Mariaziekenhuis , Overpelt , Belgium.
    Introduction: Lymphangioma accounts for 5% of benign pediatric tumors and less than 1% is located in the abdomen. While mesenteric lymphatic malformation or mesenteric lymphangioma (ML), mostly appears asymptomatic in adults, an acute clinical presentation is seen more often in children. Symptoms can mimic obstruction or peritonitis and diagnosis can therefore be challenging. Read More

    Treatment of Tongue Lymphangioma with Intralesional Combination Injection of Steroid, Bleomycin and Bevacizumab.
    Arch Craniofac Surg 2017 Mar 25;18(1):54-58. Epub 2017 Mar 25.
    Department of Plastic Surgery, Kyung Hee University College of Medicine, Seoul, Korea.
    Lymphangioma is a congenital malformed lymphatic tumor that rarely involves the tongue. In our clinic, a 10-year-old female presented with lymphangioma circumscriptum involving the right two-thirds of the tongue. We administered an intralesional combination injection of triamcinolone, bleomycin, and bevacizumab as a treatment. Read More

    A rare case of giant mesenteric cystic lymphangioma of the small bowel in an adult: A case presentation and literature review.
    Acta Gastroenterol Belg 2016 Sep-Dec;79(3):491-493
    Background : Lymphangiomas are tumours that are often found in the head and neck in children and, rarely, in adults. Among all lymphangiomas in adults, the small bowel mesentery type accounts for less than 1%. We aim to present a rare case of small bowel symptomatic cystic lymphangioma in an adult patient, as well as its diagnosis and subsequent treatment. Read More

    Malignant perivascular epithelioid cell tumor of the orbit: Report of a case and review of literature.
    Indian J Ophthalmol 2017 Sep;65(9):889-891
    Department of Ocular Pathology, Sankara Nethralaya, Medical Research Foundation, Chennai, Tamil Nadu, India.
    Perivascular epithelioid cell tumor (PEComa) is a rare neoplasm considered to arise from myomelanocytic cell lineage. The uterus is reportedly the most common site to be involved. Orbital PEComa is extremely rare with only two cases reported till date. Read More

    When Fever, Leukocytosis, and Right Lower Quadrant Pain Is Not Appendicitis.
    Pediatr Emerg Care 2017 Sep;33(9):e46-e47
    From the *Emergency Medicine Attending, and †Division of Emergency Medicine, Maimonides Medical Center, Brooklyn, NY.
    Mesenteric cystic lymphangioma (MCL) is an uncommon, benign, slow-growing abdominal tumor that is derived from the lymphatic vessels (World J Gastroenterol. 2012;18:6328-6332, Radiographics. 1994;14:729-737). Read More

    A Rare Cause of Dyspnea: Cervicothoracic Cystic Lymphangioma.
    J Craniofac Surg 2017 Sep 1. Epub 2017 Sep 1.
    *Department of Thoracic and Cardiovascular Surgery, St Vincent's Hospital, College of Medicine, The Catholic University of Korea †Department of Thoracic and Cardiovascular Surgery, Incheon St Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
    I read with great interest the article reported by Efe et al in Journal of Cranofacial Surgery (2016;27:1802-1803), presenting the excellent result obtained by the use of sclerotherapy with single-dose OK-432 in a growing cervical lymphangioma. Cervicothoracic lymphangioma is a rare congenital anomaly that is mostly asymptomatic. We would like to share our experience of a rare cause of dyspnea by lymphangioma. Read More

    Transient Reactive Eruptive Lymphangiectasia Following Partial Vulvectomy for Chronic Acquired Lymphangioma.
    Skinmed 2017 1;15(4):311-313. Epub 2017 Aug 1.
    Division of Dermatologic Surgery and Dermatopathology, Department of Dermatology, Buffalo Medical Group, Buffalo, NY.
    A 64-year-old white woman was originally diagnosed with histiocytic lymphoma in 1977. She had bilateral lymph node biopsies of the groin, chemotherapy, and radiation therapy after her diagnosis had been confirmed pathologically. She was treated with prednisone and vincristine. Read More

    Current Status, Pitfalls and Future Directions in the Diagnosis and Therapy of Lymphatic Malformation.
    J Biophotonics 2017 Aug 29. Epub 2017 Aug 29.
    Department of Otolaryngology - Head and Neck Surgery, University of Arkansas for Medical Sciences, 4301 W. Markham St, Little Rock, AR, USA, 72205.
    Lymphatic malformations (LM) are complex congenital vascular lesions composed of dilated, abnormal lymphatic channels of varying size that can result in significant aesthetic and physical impairment due to relentless growth. LMs comprised of micro-lymphatic channels (microcystic) integrate and infiltrate normal soft tissue, leading to a locally invasive mass. Ultrasonography (US) and magnetic resonance imaging (MRI) assist in the diagnosis but are unable to detect microvasculature present in microcystic LM. Read More

    Cardiac Lymphangioma Encasing Right Coronary Artery in an Infant.
    Ann Thorac Surg 2017 Sep;104(3):e279-e281
    Division of Pediatric Cardiology, Children's Hospital of Michigan, Detroit, Michigan.
    Cardiac lymphangioma is a rare primary benign tumor of the heart. We report a 3-year-old with cystic lymphangioma encasing the right coronary artery. Cardiac magnetic resonance imaging confirmed a intra-pericardial heterogeneous mass measuring 2. Read More

    Isolated cranio-orbitofacial neurofibroma mimicking vascular malformation.
    Orbit 2017 Aug 18:1-4. Epub 2017 Aug 18.
    d Dept. of Ophthalmology , School of Medicine, University of California, Davis , Sacramento , California , USA.
    Isolated neurofibromas in the absence of systemic neurofibromatosis are known as solitary or localized neurofibromas. When present in the orbit, these lesions may appear clinically and radiographically similar to other tumors, complicating diagnosis and management. Key radiographic signs may guide clinicians to the correct diagnosis when the presentation and patient demographic data obfuscate the disease entity. Read More

    [Perirenal cystic lymphangioma in an adult: a case report and literature review].
    Beijing Da Xue Xue Bao 2017 Aug;49(4):730-732
    Department of Urology, Peking University Third Hospital, Beijing 100191, China.
    Lymphangioma is a rare, benign mesenchymal neoplasm, which is characterized by numerous intercommunicating cystic spaces containing lymphatic fluid. It is considered a congenital disease resulting from the obstruction of regional lymph drainage during the developmental period. Lymphangioma frequently occurs in the cervical neck and axilla, also in the retroperitoneum, mediastinum, mesentery, omentum, colon, and pelvis, rarely in the perirenal space. Read More

    Fibroepithelial polyp of the vulva accompanied by lymphangioma circumscriptum.
    Obstet Gynecol Sci 2017 Jul 14;60(4):401-404. Epub 2017 Jul 14.
    Department of Obstetrics and Gynecology, CHA Bundang Medical Center, CHA University, Seongnam, Korea.
    Fibroepithelial polyp (FEP) and lymphangioma circumscriptum (LC) of the vulva are rare diseases that occur generally in young to middle-aged women. The pathogenesis of FEP is not clearly understood. Several previous cases have suggested that a hormonal influence may be a predisposing condition for developing FEP with or without chronic inflammation. Read More

    Small Intestinal Lymphangioma Presenting as an Acute Abdomen with Relevant Review of Literature.
    J Clin Diagn Res 2017 Jun 1;11(6):PD01-PD02. Epub 2017 Jun 1.
    Professor, Department of Paediatric Surgery, IMS BHU, Varanasi, Uttar Pradesh, India.
    Cystic lymphangioma of small bowel mesentery is rare with clinical features ranging from an asymptomatic abdominal lump to acute intestinal obstruction. We discuss two cases of lymphangioma of small bowel mesentery who presented to us as acute intestinal obstruction. In the first case exploratory laparotomy revealed a large multicystic lesion arising from small bowel mesentery just distal to the duodenojejunal junction having multiple small cysts filled with milky white fluid. Read More

    Multiple Verrucous Hemangiomas: A Case Report with New Therapeutic Insight.
    Indian Dermatol Online J 2017 Jul-Aug;8(4):254-256
    Department of Dermatology, Venereology and Leprosy, Post Graduate Institute of Medical Education and Research (PGIMER) and Dr. Ram Manohar Lohia Hospital, New Delhi, India.
    Verrucous hemangioma is an uncommon congenital vascular malformation, which may clinically masquerade angiokeratoma, lymphangioma circumscriptum, or malignant melanoma. Differentiation is essential owing to varied therapeutic and prognostic implications. We present a rare case of multiple verrucous hemangiomas in a teenage girl who presented with multiple warty lesions over the dorsal aspect of the left foot since birth. Read More

    The Public Health Burden of Lymphatic Malformations in Children: National Estimates in the United States, 2000-2009.
    Lymphat Res Biol 2017 Jul 31. Epub 2017 Jul 31.
    3 Pediatric Urology, Division of Urology, Department of Surgery, Duke University Medical Center , Durham, North Carolina.
    Objective: Describe inpatient resource utilization trends in children with lymphatic malformations using a national database.

    Data Source: Kids' inpatient database, years 2000-2009.

    Methods: Subjects included children 18 years and under with International Classification of Diseases (ICD), 9th revision code: 228. Read More

    Dermoscopy of lymphangioma circumscriptum: A morphological study of 45 cases.
    Australas J Dermatol 2017 Jul 28. Epub 2017 Jul 28.
    Department of Dermatology, General University Hospital of Alicante, Alicante, Spain.
    Background/objectives: The dermoscopy of lymphangioma circumscriptum, also known as superficial lymphatic malformation, remains to be clarified.

    Methods: Digital dermoscopic images of 45 histopathologically confirmed cases of lymphangioma circumscriptum collected from nine hospitals in Spain, Italy and Turkey were evaluated for the presence of dermoscopic structures and patterns.

    Results: Our study shows that the most common structure found in lymphangioma circumscriptum was the presence of lacunae (89% of cases). Read More

    Neonatal solid tumors.
    Pediatr Neonatol 2017 Jul 11. Epub 2017 Jul 11.
    Meenakshi Mission Hospital and Research Centre, Madurai, India. Electronic address:
    Background: Neonatal tumors are different from tumors of the older children and knowledge gained from treating older children can not be extrapolated to neonates. Neonates have immature physiology and their haematopoietic and immune systems are not fully developed and the response to therapy is unpredictable. Hence it is imperative to study these tumors as separate entity. Read More

    A large retroperitoneal lymphatic malformation successfully treated with traditional Japanese Kampo medicine in combination with surgery.
    Surg Case Rep 2017 Dec 17;3(1):80. Epub 2017 Jul 17.
    Department of Pediatric Surgery, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, 305-8575, Ibaraki, Japan.
    Background: Current treatment options for lymphatic malformations (LMs) are multimodal. Recently, the effectiveness of treating LMs with Eppikajyutsuto (TJ-28) has been reported. TJ-28 is a kind of oral herbal medicine classified as the traditional Japanese Kampo medicine. Read More

    Malignant mesenchymal neoplasms of the dermis and subcutis mimicking benign lesions: a case-based review.
    Virchows Arch 2017 Jul 12. Epub 2017 Jul 12.
    Department of Pathology, NHS Lothian University Hospitals Trust and University of Edinburgh, Edinburgh, UK.
    In this short review, malignant mesenchymal neoplasms of the dermis and subcutis mimicking benign lesions and their differential diagnoses are discussed. These include plaque-like dermatofibrosarcoma protuberans, superficial low-grade fibromyxoid sarcoma, low-grade superficial malignant peripheral nerve sheath tumour, epithelioid sarcoma, pseudomyogenic haemangioendothelioma, Kaposi sarcoma mimicking cavernous haemangioma and benign lymphangioendothelioma, and rare forms of angiosarcoma mimicking a benign vascular lesion. Read More

    [Ectopic thymus: A rare cause of neck mass in children].
    Arch Pediatr 2017 Aug 8;24(8):743-746. Epub 2017 Jul 8.
    Service ORL et chirurgie cervico-faciale, CHU Habib-Bourguiba 3029 Sfax, Tunisie.
    Introduction: Ectopic cervical thymus (ECT) is a rare embryological abnormality in children. It can be revealed by a compressive neck mass mistaken for a malignant tumor. Through a new case of ECT, we review the embryopathogenesis, diagnostic difficulties and therapeutic features. Read More

    Microbubbles in macrocysts - Contrast-enhanced ultrasound assisted sclerosant therapy of a congenital macrocystic lymphangioma: a case report.
    BMC Med Imaging 2017 Jul 6;17(1):39. Epub 2017 Jul 6.
    Department of Pediatrics and Adolescent Medicine, University Hospital of Erlangen, Loschgestrasse 15, D-91054, Erlangen, Germany.
    Background: Congenital cystic lymphangiomas are benign malformations due to a developmental disorder of lymphatic vessels. Besides surgical excision, sclerosant therapy of these lesions by intracavitary injection of OK-432 (Picibanil®), a lyophilized mixture of group A Streptococcus pyogenes, is a common therapeutical option. For an appropriate application of OK-432, a detailed knowledge about the structure and composition of the congenital cystic lymphangioma is essential. Read More

    An Uncommon Case of Cervical Thymopharyngeal Duct Cyst.
    J Clin Diagn Res 2017 May 1;11(5):PD01-PD02. Epub 2017 May 1.
    Head, Department of Paediatric Surgery, Karamandaneion Children's Hospital, Patras, Achaia, Greece.
    Thymopharyngeal duct cyst is one of the most uncommon benign cervical lesions encountered in the paediatric population. Due to its rarity, it almost always escapes a correct preoperative diagnosis and is usually misdiagnosed as a branchial cyst or lymphangioma. Furthermore, although located at the neck it may present with retrosternal or mediastinal extension. Read More

    Large Omental Cystic Lymphangioma Masquerading as Mucinous Ovarian Neoplasia in an 8-Year-Old Premenarchal Girl: The Findings from Diagnostic Imaging and Laparoscopic-Assisted Excision.
    J Pediatr Adolesc Gynecol 2017 Jun 16. Epub 2017 Jun 16.
    Department of Obstetrics and Gynecology, Gifu Prefectural Tajimi Hospital, Tajimi, Gifu, Japan.
    Background: Omental cystic lymphangioma is an extremely rare abdominal mass caused by congenital malformation.

    Case: An 8-year-old premenarchal girl reported abdominal pain. Diagnostic imaging revealed a large multicystic mass measuring 22 cm in diameter, which occupied the entire abdominal cavity with ascites. Read More

    [Pediatric salivary gland tumors and tumor-like lesions].
    Pathologe 2017 Jul;38(4):294-302
    Klinik für Hals‑, Nasen- und Ohrenheilkunde (HNO), Klinikum Augsburg, Sauerbruchstraße 6, 86156, Augsburg, Deutschland.
    Salivary gland tumors and tumor-like lesions in the pediatric population are uncommon. They comprise a heterogeneous group of infectious/inflammatory and neoplastic conditions. Pediatric salivary neoplasms include benign tumors of mesenchymal or epithelial origin as well as malignancies of epithelial (carcinomas), mesenchymal (sarcoma) or hematolymphoid (lymphoma) derivation. Read More

    Oral foregut duplication cysts: A rare and fascinating congenital lesion. Case report and review of the literature.
    Am J Otolaryngol 2016 Nov 23. Epub 2016 Nov 23.
    Department of Pathology, Louisiana State University Health Science Center, Shreveport, LA 71130, USA.
    Oral foregut duplication cysts are extremely rare lesions with approximately 57 cases reported. They are congenital cysts, located in the anterior or ventral tongue, and occur predominantly in males. They are lined by one or more types of epithelia which is limited to gastric, intestinal or respiratory epithelium. Read More

    WITHDRAWN: Role of Intralesional Bleomycin in Orbital Lymphangioma: A Prospective Study.
    J AAPOS 2017 Jun 1. Epub 2017 Jun 1.
    Dept. of Oculoplasty, Orbit, Reconstructive and Aesthetic Services, Sankara Nethralaya, Medical Research Foundation, No. 18, College Road, Chennai- 600006, Tamil Nadu, India.
    The Publisher regrets that this article is an accidental duplication of an article that has already been published, Read More

    Rapidly growing cystic hygroma in an adult patient.
    Asian Cardiovasc Thorac Ann 2017 Jun 26;25(5):395-397. Epub 2017 May 26.
    2 Department of Thoracic Surgery, Medeniyet University Goztepe Training and Research Hospital, Istanbul, Turkey.
    Cystic hygroma is a benign tumor of lymphatic tissue. It usually develops before the second year of life and is rarely seen in adults. A 26-year-old woman was referred to our clinic with a swelling in the left supraclavicular region, which had appeared 5 months earlier and grown rapidly. Read More

    Orbital Lymphangioma: Characteristics and Treatment Outcomes of 12 Cases.
    Korean J Ophthalmol 2017 Jun 12;31(3):194-201. Epub 2017 May 12.
    Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea.
    Purpose: To report the patient characteristics and treatment outcomes in 12 cases of orbital lymphangioma.

    Methods: In this study, orbital lymphangioma was diagnosed based on clinical, radiologic (computed tomography, magnetic resonance imaging), and histologic findings when possible. Patients whose vision was not compromised by orbital lymphangioma, or that did not have increased intraocular pressure (IOP), received oral corticosteroids. Read More

    Management of a Life Threatening Bleeding Following Extraction of Deciduous Second Molar Related to a Capillary Haemangioma.
    Craniomaxillofac Trauma Reconstr 2017 Jun 16;10(2):166-170. Epub 2017 Mar 16.
    Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Ain Shams University, Cairo, Egypt.
    Various forms of vascular lesion affect the head and neck region. The head and neck vascular lesions are classified into neoplasms and malformations. Neoplasm presents either as hemangioma or lymphangioma; neoplasm usually presents in young age compared with vascular malformation. Read More

    Dermoscopy of cutaneous lymphangioma circumscriptum.
    Dermatol Pract Concept 2017 Apr 30;7(2):37-38. Epub 2017 Apr 30.
    Skinnocence: The Skin Clinic, Gurgaon, India.
    Lymphangiomas are congenital lymphatic malformations. They are clinically characterized by clusters of translucent vesicles, and on dermoscopy, yellow lacunae surrounded by pale septa as well as reddish to bluish lacunae have been described. A young male presented with a seven-year history of a vesicular lesion. Read More

    Cystic Lymphangioma of the Colon: Endoscopic Removal beyond the Frontiers of Size.
    Case Rep Gastroenterol 2017 Jan-Apr;11(1):178-183. Epub 2017 Apr 10.
    Bronx Lebanon Hospital Center, Bronx, NY, USA.
    Cystic lymphangiomas are benign colonic neoplasms arising from the submucosa. Traditionally, endoscopic resection has been described for smaller lesions, while surgery is reserved for larger symptomatic lesions. We present a case of a 69-year-old asymptomatic individual noted to have a cystic lymphangioma of the colon measuring 5 cm, which was successfully removed with endoloop endoscopic resection without any complications. Read More

    Vascular lesions of the female genital tract: Clinicopathologic findings and application of the ISSVA classification.
    Pathophysiology 2017 Sep 23;24(3):161-167. Epub 2017 Apr 23.
    Department of Pathology, North Hospital, University Hospital of St-Etienne, France.
    Introduction: Vascular lesions of the female genital tract are extremely rare and their nomenclature does not widely follow the International Society for the Study of Vascular Anomalies (ISSVA) classification.

    Aim Of The Study: To describe the clinicopathologic characteristics of vascular lesions of the female genital tract and to apply the ISSVA classification.

    Material And Methods: 19 vascular lesions were diagnosed during a 20 year period. Read More

    A mesocolonic lymphangioma in an adult with peritonitis: a case report.
    J Surg Case Rep 2017 Feb 9;2017(2):rjx017. Epub 2017 Feb 9.
    Department of Surgery, JR Hiroshima Hospital, 3-1-36 Futabanosato, Higashi-ku, Hiroshima 7320057, Japan.
    Cystic lymphangiomas of the mesocolon are very rare in adults. They are usually asymptomatic, but can present with an acute abdomen. We report an adult patient with cystic lymphangioma of the mesocolon that manifested with peritonitis. Read More

    [Giant mesocolic cystic lymphangioma: A treacherous prenatal presentation. Case report].
    Arch Pediatr 2017 Jun 25;24(6):552-556. Epub 2017 Apr 25.
    Service de chirurgie pédiatrique, centre hospitalo-universitaire d'Amiens, avenue René-Laennec, 80054 Amiens cedex 1, France.
    Cystic lymphangiomas are usually located in the neck region. Less frequently, they can be found in the abdomen. In those cases, pre- and neonatal diagnosis is extremely difficult. Read More

    [A rare cause of spontaneous hemoperitoneum in adults: ruptured cystic hemolymphangioma].
    Pan Afr Med J 2017 4;26. Epub 2017 Jan 4.
    Clinique Chirurgicale des Urgences Viscérales, Hôpital Avicenne, CHU Rabat-Salé, Rabat, Maroc.
    Hemolymphangioma is a benign tumor resulting from the abnormal development of the lymphatic vessels associated with vascular malformations. 50% to 60% of these tumours are present at birth. Cervical forms are most frequent. Read More

    Sonographic findings in two cases of lymphangioma of the mesocolon in adults.
    J Clin Ultrasound 2017 Apr 25. Epub 2017 Apr 25.
    Department of Radiology, Akita Red Cross Hospital, 222-1 Kamikitade Saruta, Akita-shi, Akita, 010-1495, Japan.
    Lymphangioma of the mesocolon is very rare. We report two cases of surgically resected and histologically proven mesocolic lymphangioma in adults. In both cases, ultrasound revealed a large cystic mass with multiple thin septa in the lower abdomen. Read More

    Cystic pancreatic lymphangioma diagnosed with endoscopic ultrasound-guided fine needle aspiration.
    Endosc Ultrasound 2017 Mar-Apr;6(2):136-139
    Department of Gastroenterology and Hepatology, Changi General Hospital, Simei, Singapore.
    Pancreatic lymphangiomas are rare, but benign neoplasms. Historically, the diagnoses in various case reports were mostly made after surgical resection. There are emerging data concerning the utility of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) to differentiate it from more sinister pancreatic cystic neoplasms. Read More

    Sodium Tetradecyl Sulfate: A Review of Clinical Uses.
    Dermatol Surg 2017 Apr 19. Epub 2017 Apr 19.
    *University of Texas McGovern Medical School at Houston, Houston, Texas; †Department of Dermatology, University of Texas McGovern Medical School at Houston, Houston, Texas.
    Background: Sodium tetradecyl sulfate (STS) is Food and Drug Administration approved for treatment of varicose veins, but numerous other off-label applications have been reported.

    Objective: To describe the clinical uses of STS, as well as efficacy and adverse effects.

    Methods: Review of studies searchable on PubMed from 1938 to 2016 describing clinical uses of STS to determine efficacy and adverse effects associated with various applications. Read More

    Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis.
    Taiwan J Obstet Gynecol 2017 Apr;56(2):230-233
    Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan; Department of Bioengineering, Tatung University, Taipei, Taiwan.
    Objective: We present cytogenetic and molecular cytogenetic diagnoses of mosaic deletion of chromosome 15q11.1-q11.2 in a fetus with diffuse lymphangiomatosis. Read More

    1 OF 130