3,534 results match your criteria Hemangioma Capillary

Primary and secondary retinal capillary haemangioma in Mexico.

Arch Soc Esp Oftalmol (Engl Ed) 2021 Jun 2;96(6):337-341. Epub 2020 Aug 2.

Departamento de Retina & Vítreo, Fundación Hospital "Nuestra Señora de la Luz", I.A.P., Mexico City, Mexico.

A series is presented of sixteen cases of retinal capillary haemangioma (RCH) from consecutive patients at an ophthalmology teaching hospital in Mexico City. There were seven primary haemangioblastomas, and nine due to von Hippel-Lindau disease (VHL). All cases associated with VHL already had systemic manifestations, such as, cerebellar, medullary and renal tumours. Read More

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A Case Report of Multiple Capillary Hemangioma in a Chronic Myeloid Leukemia Patient Taking Tyrosine Kinase Inhibitors.

Ann Dermatol 2021 Jun 4;33(3):278-280. Epub 2021 May 4.

Department of Dermatology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

A capillary hemangioma is a vascular tumor with small capillary sized vascular channel. Multiple capillary hemangioma in relation with drugs have been rarely reported. Here in, we report a case of multiple capillary hemangioma in patient diagnosed with chronic myeloid leukemia who received tyrosine kinase inhibitors (TKIs). Read More

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Baseline description of the Spanish Academy of Dermatology infantile haemangioma nationwide prospective cohort. Comparison of patients treated with propranolol in routine clinical practice with previous pivotal clinical trial data.

Actas Dermosifiliogr 2021 May 27. Epub 2021 May 27.

Departamento de Dermatología, Hospital Virgen del Rocío, Sevilla, España; Departamento de Dermatología, Hospital Viamed Santa Ángela de la Cruz, Sevilla, España.

Background: There are several therapeutic options for infantile haemangiomas (IH). Propranolol is used according to a pivotal trial. We aimed to describe the characteristics of IH in clinical practice, including the therapies used, and to compare the characteristics of patients treated with propranolol with those of the trial to assess its external validity. Read More

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Retinal racemose hemangioma (retinal arteriovenous communication) diagnosed and managed with multimodal imaging.

Retin Cases Brief Rep 2021 May 1. Epub 2021 May 1.

Vitreous Retina Macula Consultants of New York, New York, NY, USA Columbia University College of Physicians and Surgeons, New York, NY, USA New York University, Department of Ophthalmology, New York, NY, USA Manhattan Eye, Ear, and Throat Hospital, Lenox Hill Hospital, New York, NY, USA Wilmer Eye Institute, Johns Hopkins Hospital, Johns Hopkins University School of Medicine, Baltimore, MD, USA Institute of Ophthalmology, Fundación Conde de Valenciana, Mexico City, Mexico Ophthalmology Unit, Department of Medicine, Surgery and Neuroscience, University of Siena, Siena University Hospital, Siena, Italy Department of Ophthalmology, Hofstra Northwell School of Medicine, Hempstead, NY, USA.

Purpose: Retinal racemose hemangioma (RRH) is a rare congenital abnormality of the retinal vasculature with a variety of secondary manifestations that can cause vision loss, including macular edema. This report aims to demonstrate the utility of swept-source optical coherence tomography angiography (SS-OCTA) in further characterizing this abnormality.

Methods: Case report with multimodal imaging including SS-OCTA. Read More

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Giant left atrial capillary haemangioma invading left-main coronary artery.

Interact Cardiovasc Thorac Surg 2021 May 17. Epub 2021 May 17.

Department of Cardiovascular Surgery, Necmettin Erbakan University, Meram Medicine Faculty, Konya, Turkey.

Cardiac haemangiomas are rare cases and can be seen at any age of life. A 49-year-old woman was admitted to our hospital with chest pain. A well-circumscribed soft tissue mass extending from the pulmonary artery truncus to the left ventricular inferior neighborhood. Read More

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Ultrasonographic features of an intravascular lobular capillary hemangioma originating in the basilic vein: Case report and literature review.

J Clin Ultrasound 2021 May 12. Epub 2021 May 12.

Department of Ultrasound Medicine, West China Hospital, Sichuan University, Chengdu, China.

Intravascular lobular capillary hemangioma (ILCH) is a rare variant of pyogenic granuloma, which develops within the lumen of a blood vessel. Here, we report the case of a 38-year-old male presenting with a mobile, incompressible, nonpulsatile nodule in the superficial fascia of the forearm. A first ultrasonographic examination diagnosed the mass as intravascular thrombosis with partial recanalization. Read More

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Multifocal pleural capillary hemangioma: a rare cause of hemorrhagic pleural effusion-case report.

BMC Pulm Med 2021 May 10;21(1):156. Epub 2021 May 10.

Department of Respiratory Disease, Daping Hospital, Army Medical University, Chongqing, 400042, China.

Background: Capillary hemangioma can be found in many organs, but rarely in pleura. Previously, only localized pleural capillary hemangioma cases have been reported. Corticosteroids are the most commonly recommended drugs in capillary hemangioma. Read More

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Intravenous Lobular Capillary Haemangioma (Pyogenic Granuloma) of the Superior Vena Cava: Case Report and Literature Review.

EJVES Vasc Forum 2021 24;50:32-36. Epub 2020 Dec 24.

Department of Vascular Surgery and Kidney Transplantation, University of Strasbourg, France.

Introduction: Intravascular lobular capillary haemangioma is a rare benign intravascular tumour, especially in large vessels. This is the report of a case and associated literature review.

Report And Literature Review: This is the report of the first case of an intravenous lobular capillary haemangioma (ILCH) of the superior vena cava (SVC). Read More

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December 2020

Clitoromegaly, Vulvovaginal Hemangioma Mimicking Pelvic Organ Prolapse, and Heavy Menstrual Bleeding: Gynecologic Manifestations of Klippel-Trénaunay Syndrome.

Medicina (Kaunas) 2021 Apr 9;57(4). Epub 2021 Apr 9.

Department of Obstetrics and Gynecology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul 05505, Korea.

Klippel-Trénaunay Syndrome (KTS) is a genetic vascular malformation involving the capillary, lymphatic, and venous channels. Prenatal sonographic diagnosis of KTS with an enlarged fetal limb is well-known; however, postnatal gynecologic manifestations are rarely reported. KTS can cause clitoromegaly, vulvovaginal hemangioma, and heavy menstrual bleeding. Read More

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[Clinicopathological study of infantile hemangioma].

Zhonghua Bing Li Xue Za Zhi 2021 May;50(5):508-510

Department of Hemangioma, Henan Provincial People's Hospital, Zhengzhou 450003, China.

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Verrucous Venous Malformation-Subcutaneous Variant.

Am J Dermatopathol 2021 Apr 21. Epub 2021 Apr 21.

Department of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, MA; Department of Pathology, Institute Curie, Paris, France; Division of Plastic Surgery, Department of Surgery, University of Pennsylvania, Philadelphia, PA; Department of Dermatology, Boston Children's Hospital and Harvard Medical School, Boston, MA; Department of Radiology, Boston Children's Hospital and Harvard Medical School, Boston, MA; Department of Plastic and Oral Surgery, Boston Children's Hospital and Harvard Medical School, Boston, MA; Department of Orthopaedics, Beth Israel Deaconess Medical Center, Boston, MA; Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, MA; and Department of Orthopedics, Boston Children's Hospital and Harvard Medical School, Boston, MA.

Background: Verrucous venous malformation (VVM), previously called "verrucous hemangioma," typically involves the dermis and the subcutaneous fat. We have encountered patients with VVM confined to the hypodermis.

Materials And Methods: During a nearly 20-year period, 13 patients, aged 2-17 years, presented with a subcutaneous mass in the limb without clinically obvious epidermal alterations. Read More

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Postcricoid haemangioma with laryngomalacia in infancy.

BMJ Case Rep 2021 Apr 19;14(4). Epub 2021 Apr 19.

Department of Otorhinolaryngology Head & Neck Surgery, Universiti Kebangsaan Malaysia Medical Centre, Bandar Tun Razak, Wilayah Persekutuan Kuala Lumpur, Malaysia

Infantile haemangioma represents a congenital vascular anomaly commonly observed in the head and neck region. Such an occurrence over the postcricoid region, however, is rather unusual. Herein, the authors report a case of a synchronous postcricoid haemangioma in a 7-week-old newborn diagnosed with severe laryngomalacia. Read More

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[Duodenal capillary hemangioma as an atypical cause of iron deficiency. Case report].

An Sist Sanit Navar 2021 Apr 28;44(1):119-122. Epub 2021 Apr 28.

Servicio de Digestivo. Complejo Hospitalario de Navarra. Pamplona..

Hemangiomas are benign vascular gastrointestinal tumours. They are infrequent, located in the submucosa, and can be asymptomatic or cause intestinal obstruction, anaemia or ferropenia. Their initial diagnosis is usually endoscopic despite the absence of pathognomonic features. Read More

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Lobular Capillary Hemangioma Originating From the Posterior End of the Inferior Turbinate: A Very Rare Occurrence.

Jae Hoon Lee

Ear Nose Throat J 2021 Apr 13:1455613211009133. Epub 2021 Apr 13.

Department of Otolaryngology, Institute of Wonkwang Medical Science, 35030Wonkwang University School of Medicine, Iksan, Chonbuk, Republic of Korea.

Lobular capillary hemangioma mostly occurs in the anterior portion of the nasal cavity, rarely occurring in the posterior end of the inferior turbinate, as in this case. We report a case of lobular capillary hemangioma originating from the posterior end of the right inferior turbinate, which was successfully removed via an endoscopic endonasal approach. Read More

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Encephalotrigeminal Angiomatosis with Facial Lobular Capillary Hemangioma: An Unusual Case Report.

Int J Appl Basic Med Res 2021 Jan-Mar;11(1):44-46. Epub 2021 Jan 26.

Department of Oral and Maxillofacial Pathology, BVDU Dental College, Sangli, Maharashtra, India.

Encephalotrigeminal angiomatosis, also called Sturge-Weber syndrome (SWS), is a syndrome of etiology which is not yet clear. It is a nonhereditary condition. The clinical features include pigmentation over the facial skin known as port-wine stain, abnormalities of ocular region, and central nervous system involvement as leptomeningeal angioma. Read More

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January 2021

Recurrent equine capillary haemangioma treated with adjunctive laser photocoagulation therapy: a case report.

Vet Dermatol 2021 Jun 6;32(3):290-e78. Epub 2021 Apr 6.

Department of Veterinary Medicine, University of Milan, Lodi, LO, Italy.

The aim of the present work was to describe a case of recurrent capillary haemangioma at the coronary border of the left front limb in a 6-month-old thoroughbred filly successfully treated with diode laser ablation and adjunctive laser photocoagulation therapy. Read More

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Stemness-Associated Markers Are Expressed in Extracranial Arteriovenous Malformation.

Front Surg 2021 19;8:621089. Epub 2021 Mar 19.

Gillies McIndoe Research Institute, Wellington, New Zealand.

Arteriovenous malformation (AVM) consists of a with poorly formed low-resistance vessels in place of a functional capillary network. The role of somatic mutations in embryonic stem cells (ESCs) and vascular anomalies and the presence of primitive populations in vascular anomalies led us to investigate the presence of a primitive population in extracranial AVM. Extracranial AVM tissue samples from 12 patients were stained for stemness-associated markers OCT4, SOX2, NANOG, KLF4, and c-MYC using immunohistochemical staining. Read More

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Capillary haemangioma: a rare cause of iron-deficiency anaemia.

BMJ Case Rep 2021 Mar 31;14(3). Epub 2021 Mar 31.

Colorectal Surgery, South Devon Healthcare Trust, Torquay, UK.

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Ophthalmological Aspects of von-Hippel-Lindau Syndrome.

Semin Ophthalmol 2021 Mar 29:1-10. Epub 2021 Mar 29.

Department of Internal Medicine, King's Mill Hospital, Sutton-in-Ashfield, Nottinghamshire, UK.

von Hippel-Lindau (VHL) syndrome is a multisystem neoplastic disorder involving eyes, central nervous system, kidneys, spine, and other tissues. A retinal capillary hemangioma (RCH) is the earliest manifestation of the VHL disease in most cases.This paper aims to provide an up-to-date review of the current literature about von Hippel-Lindau syndrome. Read More

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Complete resection of pulmonary artery hemangioma on the beating heart.

J Card Surg 2021 Mar 25. Epub 2021 Mar 25.

Department of Cardiothoracic Surgery, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Cardiac hemangiomas are rare entities and very few cases have been reported where they originate from the main arteries of the heart. We present a case of hemangioma arising from the main pulmonary artery, which was completely resected with clear margins on the beating heart. Read More

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Multiple Erythematous Nodules: An Intriguing Entity.

Indian Dermatol Online J 2021 Jan-Feb;12(1):142-146. Epub 2021 Jan 16.

Department of Pathology, Government Medical College, Nagpur, Maharashtra, India.

Pyogenic granuloma (PG), also called a lobular capillary hemangioma, is a benign vascular proliferation of skin or mucous membrane. It classically presents as a solitary friable nodule over the face or distal extremities. Multiple disseminated PG is a rare form generally reported after trauma such as burn injury. Read More

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January 2021

A refractory pleural effusion caused by a pleural capillary hemangioma.

Respir Med Case Rep 2021 9;33:101384. Epub 2021 Mar 9.

Department of Thoracic Surgery, Isahaya General Hospital, Isahaya City, Nagasaki, 854-8501, Japan.

A 69-year-old man presented with a left pleural effusion. Even after repeated drainage, the pleural effusion had been increasing for more than two years. Thoracoscopy unexpectedly showed a pleural mass on the parietal pleura, and it was completely removed. Read More

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Intradural extramedullary capillary hemangioma of the cauda equina: case report of a rare spinal tumor.

Spinal Cord Ser Cases 2021 Mar 19;7(1):21. Epub 2021 Mar 19.

Department of Neurological Surgery, Thomas Jefferson University Hospital, Philadelphia, PA, USA.

Introduction: Intradural extramedullary capillary hemangiomas of the cauda equina are exceedingly rare, with only 20 previous cases reported. In the adult population, these tumors are rare and can arise in the central and peripheral nervous systems from the dura or spinal nerve roots. Intradural capillary hemangiomas of the cauda equina can yield symptoms such as lower extremity weakness, pain, and bladder and bowel dysfunction. Read More

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[Lombosacral epidural capillary hemangioma].

Rev Prat 2020 11;70(9):989

Service de radiologie, CHU Mohammed VI, Oujda, Maroc.

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November 2020

Algorithmic Approach to Fibroinflammatory Sinonasal Tract Lesions.

Head Neck Pathol 2021 Mar 15;15(1):120-129. Epub 2021 Mar 15.

Department of Pathology, Southern California Permanente Medical Group, 5601 De Soto Avenue, Woodland Hills, CA, 91365, USA.

Fibroinflammatory lesions of the sinonasal tract are one of the most common head and neck lesions submitted to surgical pathology. When the fibroinflammatory pattern represents the lesion (i.e. Read More

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Paradoxical capillary hemangioma during treatment with ramucirumab.

Dermatol Ther 2021 May 22;34(3):e14938. Epub 2021 Mar 22.

Department of Dermatology, University Hospital Complex of Santiago de Compostela, Santiago de Compostela, Spain.

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Ossifying pyogenic granuloma: A rare variant usually not recognized.

J Cutan Pathol 2021 Mar 10. Epub 2021 Mar 10.

Department of Pathology, Robert J. Tomsich Pathology and Laboratory Medicine, Cleveland Clinic, Ohio, USA.

Pyogenic granuloma (PG) represents a polypoid and lobular, capillary lesion, resembling granulation tissue, usually occurring on skin or mucosal surfaces. The occurrence of metaplastic ossification is extremely rare in PG. We present three cases of PG with metaplastic ossification. Read More

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Surgical Management of Facial Port-Wine Stain in Sturge Weber Syndrome.

Cureus 2021 Jan 11;13(1):e12637. Epub 2021 Jan 11.

Plastic and Reconstructive Surgery, Nicklaus Children's Hospital, Miami, USA.

Sturge Weber Syndrome is characterized by the classic triad of a facial port-wine stain, leptomeningeal angiomatosis, and glaucoma. The resultant facial vascular anomaly can lead to soft tissue and bone irregularities, causing psychosocial distress and mental health morbidity. When severe, patients can opt for multi-staged surgical intervention by reconstructive surgeons to restore normal symmetry and improve the aesthetic appearance of the face. Read More

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January 2021

Intracranial infantile hemangioma - rare entity and common pitfalls: A comprehensive multidisciplinary approach from Neurosurgery, Neurooncology and Neuropathology.

Clin Neuropathol 2021 Feb 9. Epub 2021 Feb 9.

Objective: To review the rare entity of pediatric intracranial hemangiomas and discuss surgical pitfalls and pathophysiology in regard to cerebral edema formation.

Materials And Methods: We describe an extremely rare case of intracranial infantile hemangioma in a neonate with massive cerebral edema, surgically resected urgently because of acute herniation. We review the literature of 46 other pediatric cases of intracranial hemangioma, including congenital capillary hemangiomas. Read More

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February 2021