Generalized lupus panniculitis and antiphospholipid syndrome in a patient without complement deficiency

Hossein C. Nousari; Arash Kimyai-Asadi; Helen M. Santana; Gerardine M. Diglio; Francisco A. Tausk; Bernard A. Cohen

doi:10.1046/j.1525-1470.1999.00060.x

Generalized lupus panniculitis and antiphospholipid syndrome in a patient without complement deficiency

Hossein C. Nousari, Arash Kimyai-Asadi, Helen M. Santana, Gerardine M. Diglio, Francisco A. Tausk, Bernard A. Cohen

Research output: Contribution to journal › Article › peer-review

17 Scopus citations

Abstract

Generalized chronic cutaneous lupus including lupus panniculitis in childhood is rare and usually occurs in the setting of genetic complement deficiencies. The association with antiphospholipid syndrome is even more rare. We report 13-year old girl with extensive lupus panniculitis since the age of 8 months and no evidence of complement deficiency. She recently developed antiphospholipid syndrome characterized by anticardiolipin antibodies and digital necrosis.

Original language	English (US)
Pages (from-to)	273-276
Number of pages	4
Journal	Pediatric Dermatology
Volume	16
Issue number	4
DOIs	https://doi.org/10.1046/j.1525-1470.1999.00060.x
State	Published - Jul 1999

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Dermatology

Access to Document

10.1046/j.1525-1470.1999.00060.x

Cite this

@article{b4d60b309dde46fd982662dc4aa1f6a0,

title = "Generalized lupus panniculitis and antiphospholipid syndrome in a patient without complement deficiency",

abstract = "Generalized chronic cutaneous lupus including lupus panniculitis in childhood is rare and usually occurs in the setting of genetic complement deficiencies. The association with antiphospholipid syndrome is even more rare. We report 13-year old girl with extensive lupus panniculitis since the age of 8 months and no evidence of complement deficiency. She recently developed antiphospholipid syndrome characterized by anticardiolipin antibodies and digital necrosis.",

author = "Nousari, {Hossein C.} and Arash Kimyai-Asadi and Santana, {Helen M.} and Diglio, {Gerardine M.} and Tausk, {Francisco A.} and Cohen, {Bernard A.}",

year = "1999",

month = jul,

doi = "10.1046/j.1525-1470.1999.00060.x",

language = "English (US)",

volume = "16",

pages = "273--276",

journal = "Pediatric Dermatology",

issn = "0736-8046",

publisher = "Wiley",

number = "4",

}

TY - JOUR

T1 - Generalized lupus panniculitis and antiphospholipid syndrome in a patient without complement deficiency

AU - Nousari, Hossein C.

AU - Kimyai-Asadi, Arash

AU - Santana, Helen M.

AU - Diglio, Gerardine M.

AU - Tausk, Francisco A.

AU - Cohen, Bernard A.

PY - 1999/7

Y1 - 1999/7

N2 - Generalized chronic cutaneous lupus including lupus panniculitis in childhood is rare and usually occurs in the setting of genetic complement deficiencies. The association with antiphospholipid syndrome is even more rare. We report 13-year old girl with extensive lupus panniculitis since the age of 8 months and no evidence of complement deficiency. She recently developed antiphospholipid syndrome characterized by anticardiolipin antibodies and digital necrosis.

AB - Generalized chronic cutaneous lupus including lupus panniculitis in childhood is rare and usually occurs in the setting of genetic complement deficiencies. The association with antiphospholipid syndrome is even more rare. We report 13-year old girl with extensive lupus panniculitis since the age of 8 months and no evidence of complement deficiency. She recently developed antiphospholipid syndrome characterized by anticardiolipin antibodies and digital necrosis.

UR - http://www.scopus.com/inward/record.url?scp=0032816233&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0032816233&partnerID=8YFLogxK

U2 - 10.1046/j.1525-1470.1999.00060.x

DO - 10.1046/j.1525-1470.1999.00060.x

M3 - Article

C2 - 10469410

AN - SCOPUS:0032816233

SN - 0736-8046

VL - 16

SP - 273

EP - 276

JO - Pediatric Dermatology

JF - Pediatric Dermatology

IS - 4

ER -

Generalized lupus panniculitis and antiphospholipid syndrome in a patient without complement deficiency

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this