Document Detail


Systemic involvement in scleredema of Buschke associated with IgG-kappa paraproteinaemia.
MedLine Citation:
PMID:  9217831     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Scleredema is a rare primary cutaneous mucinosis. Systemic involvement is uncommon and histological confirmation is often lacking. We report a case of a 60-year-old man with scleredema and evidence of mucin deposition on biopsies from multiple extracutaneous sites. The bone marrow, nerve, hepatic and salivary gland involvement seen on histology in our patient has not, to our knowledge, been previously reported in this condition.
Authors:
T Basarab; N P Burrows; S E Munn; R Russell Jones
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The British journal of dermatology     Volume:  136     ISSN:  0007-0963     ISO Abbreviation:  Br. J. Dermatol.     Publication Date:  1997 Jun 
Date Detail:
Created Date:  1997-07-29     Completed Date:  1997-07-29     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0004041     Medline TA:  Br J Dermatol     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  939-42     Citation Subset:  IM    
Affiliation:
Department of Dermatology, Ealing Hospital, Southall, Middlesex, UK.
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MeSH Terms
Descriptor/Qualifier:
Bone Marrow / pathology
Humans
Immunoglobulin G*
Liver / pathology
Male
Middle Aged
Mouth Mucosa / pathology
Nerve Tissue / pathology
Paraproteinemias / complications*,  pathology
Salivary Glands / pathology
Scleredema Adultorum / immunology*,  pathology
Skin / pathology
Chemical
Reg. No./Substance:
0/Immunoglobulin G

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


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