Document Detail

Localized scleroderma: a series of 52 patients.
MedLine Citation:
PMID:  19393504     Owner:  NLM     Status:  MEDLINE    
BACKGROUND: Localized scleroderma also called morphea is a skin disorder of undetermined cause. The widely recognized Mayo Clinic Classification identifies 5 main morphea types: plaque, generalized, bullous, linear and deep. Whether each of these distinct types has a particular clinical course or is associated with some patient-related features is still unclear. METHODS: We report here a retrospective series of patients with localized scleroderma with an attempt to identify features related to the type of lesion involved. The medical records of all patients with a diagnosis of localized scleroderma were reviewed by skilled practitioners. Lesions were classified according to the Mayo Clinic Classification. The relationship between each lesion type and various clinical features was tested by non-parametrical methods. RESULTS: The sample of 52 patients included 43 females and 9 males. Median age at onset was 30 y (range 1-76). Frequencies of patients according to morphea types were: plaque morphea 41 (78.8%) (including morphea en plaque 30 (57.7%) and atrophoderma of Pasini-Pierini 11 (21.1%)), linear scleroderma 14 (26.9%). Nine patients (17.3%) had both types of localized scleroderma. Median age at onset was lower in patients with linear scleroderma (8 y (range 3-44)) than in others (36 y (range 1-77)) (p=0.0003). Head involvement was more common in patients with linear scleroderma (37.5%) than in other subtypes (11.1%) (p=0.05). Atrophoderma of Pasini-Pierini was never located at the head. Systemic symptoms, antinuclear antibodies and the rheumatic factor were not associated with localized scleroderma types or subtypes. CONCLUSION: These results suggest that morphea types, in adults are not associated with distinct patient features except for age at disease onset (lower) and the localization on the head (more frequent), in patients with lesions of the linear type.
C Toledano; S Rabhi; A Kettaneh; B Fabre; L Fardet; K P Tiev; J Cabane
Related Documents :
14648024 - All- trans-retinoic acid-induced erythema nodosum in patients with acute promyelocytic ...
20161854 - The 'holi' dermatoses: annual spate of skin diseases following the spring festival in i...
12043764 - Do warming blankets increase bacterial counts in the operating field in a laminar-flow ...
18070024 - Cutaneous manifestations in relation to immunologic parameters in a cohort of primary m...
17603764 - Multiple sclerosis and headache co-morbidity. a case-control study.
19816624 - Adherence to guidelines for surveillance colonoscopy in patients with ulcerative coliti...
Publication Detail:
Type:  Journal Article     Date:  2008-09-17
Journal Detail:
Title:  European journal of internal medicine     Volume:  20     ISSN:  1879-0828     ISO Abbreviation:  Eur. J. Intern. Med.     Publication Date:  2009 May 
Date Detail:
Created Date:  2009-04-27     Completed Date:  2009-07-22     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9003220     Medline TA:  Eur J Intern Med     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  331-6     Citation Subset:  IM    
Department of Internal Medicine Centre Hospitalo-Universitaire Saint-Antoine, 75012 Paris, Assistance Publique/Hôpitaux de Paris, France.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Age of Onset
Child, Preschool
Middle Aged
Retrospective Studies
Scleroderma, Localized / classification*,  drug therapy,  pathology*
Skin / pathology*
Steroids / therapeutic use
Subcutaneous Tissue / pathology
Young Adult
Reg. No./Substance:

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

Previous Document:  A French national research project to the creation of an auscultation's school: the ASAP project.
Next Document:  Magnetic compression biliary-enteric anastomosis for palliation of obstructive jaundice: initial cli...