Document Detail


Glomeruloid hemangioma. A cutaneous marker of POEMS syndrome.
MedLine Citation:
PMID:  8030771     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Glomeruloid hemangioma is a histologically distinctive cutaneous hemangioma that recently has been associated with POEMS syndrome. We report a further case in which POEMS syndrome was signaled by multiple eruptive angiomas of the glomeruloid type. Histopathology showed multiple dilated vascular spaces containing a conglomerate of capillaries resulting in a structure resembling renal glomeruli. Eosinophilic globules, probably representing immunoglobulins, were found within the cytoplasm of some endothelial and stromal cells. The finding of focal histologic features of tufted angioma (angioblastoma) in the same lesion suggests that a spectrum of hemangiomatous lesions may be seen in POEMS syndrome. Alternatively, glomeruloid hemangioma may represent a reactive endothelial proliferation rather than a neoplastic lesion.
Authors:
F Rongioletti; C Gambini; R Lerza
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The American Journal of dermatopathology     Volume:  16     ISSN:  0193-1091     ISO Abbreviation:  Am J Dermatopathol     Publication Date:  1994 Apr 
Date Detail:
Created Date:  1994-08-11     Completed Date:  1994-08-11     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7911005     Medline TA:  Am J Dermatopathol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  175-8     Citation Subset:  IM    
Affiliation:
University of Genoa, Department of Dermatology, Italy.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Hemangioma / pathology*
Humans
Male
Middle Aged
POEMS Syndrome / pathology*
Skin / pathology
Skin Neoplasms / pathology*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Melanoma in situ on facial skin damaged by sunlight.
Next Document:  Atypical beta 2-microglobulin amyloidosis following short-term hemodialysis.