Glomeruloid Hemangioma as a Marker for the Early Diagnosis of POEMS Syndrome
نویسندگان
چکیده
Vol. 29, No. 2, 2017 249 Received March 16, 2015, Revised February 29, 2016, Accepted for publication April 25, 2016 Corresponding author: Sang Seok Kim, Department of Dermatology, Hallym University Kangdong Sacred Heart Hospital, Hallym University College of Medicine, 150 Seongan-ro, Gangdong-gu, Seoul 05355, Korea. Tel: 82-2-2224-2285, Fax: 82-2-474-7913, E-mail: [email protected] This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Copyright © The Korean Dermatological Association and The Korean Society for Investigative Dermatology https://doi.org/10.5021/ad.2017.29.2.249
منابع مشابه
DERMATOPATHOLOGY Glomeruloid hemangioma in POEMS syndrome: a report on two cases and a review of the literature
Glomeruloid hemangioma is characterized by coiled capillary vessels contained within enlarged vascular spaces displaying an architecture that resembles renal glomeruli. The condition is strongly associated with POEMS syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal gammopathy and Skin changes). The present paper reports on two cases of glomeruloid hemangiomas associated with P...
متن کاملGlomeruloid hemangioma in POEMS syndrome: a report on two cases and a review of the literature.
Glomeruloid hemangioma is characterized by coiled capillary vessels contained within enlarged vascular spaces displaying an architecture that resembles renal glomeruli. The condition is strongly associated with POEMS syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal gammopathy and Skin changes). The present paper reports on two cases of glomeruloid hemangiomas associated with P...
متن کاملAn unusual presentation of glomeruloid hemangioma in a patient with VHL syndrome: A case report and review of literature
Von Hippel-Lindau (VHL) is an inherited neoplasia syndrome caused by inactivation of the VHL tumor suppressor gene, characterized by the development of sporadic clear cell renal carcinoma, pheochromocytomas, retinal angioma, pancreatic cysts, and CNS hemangioblastomas. Glomeruloid hemangioma is a vascular lesion, previously considered to be specifically associated with POEMS (polyneuropathy, or...
متن کاملGlomeruloid haemangiomas associated with generalized oedema in a patient with atypical POEMS syndrome
A 55-year-old woman was admitted for evaluation of progressive generalized oedema and mild kidney dysfunction (serum creatinine 1.12mg/dL; blood urea nitrogen 45mg/dL). On admission, generalized oedema, transudative pleural effusion, collapsed inferior vena cava and low fractional excretion of sodium (0.14%) suggested severe volume depletion due to plasma extravasation; however, its aetiology c...
متن کاملPOEMS syndrome associated with multiple hemangiomas of the small bowel and colon.
thy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes. POEMS syndrome is a rare disor− der, with only a limited number of cases reported in the literature. The first de− scriptions of POEMS syndrome were pub− lished by Crow in 1956 [1] and by Fukase in 1968 [2]. It is therefore also known as Crow±Fukase syndrome. The symptom complex of POEMS syndrome includes skin changes s...
متن کامل