Anti-centromere antibody-positive subjects presenting with hypertensive emergency and renal dysfunction in the absence of skin manifestations: A variant of systemic sclerosis or a novel entity?

5Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.

Abstract

Two patients with anti-centromere antibody (ACA), hypertensive emergency, and acute renal failure, mimicking scleroderma renal crisis, without Raynaud's phenomenon and typical skin manifestations of systemic sclerosis (SSc), are reported. A review of 26 ACA-positive patients between March 2003 and March 2011 in Yokosuka Kyosai Hospital identified four additional patients with similar manifestations. All patients were Japanese women between 41 and 84 years of age at presentation. Human leukocyte antigen (HLA) genotyp-ing tests revealed the absence of the HLA-DQB1*0501 and DRB1*0101 alleles, which are associated with disease susceptibility to ACA-positive SSc among Japanese. These subjects' manifestations may represent a novel entity. © 2012 The Japanese Society of Internal Medicine.

Cite

CITATION STYLE

APA

Mandai, S., Arai, Y., Hirasawa, S., Hirai, T., Aki, S., Inaba, N., … Sasaki, S. (2012). Anti-centromere antibody-positive subjects presenting with hypertensive emergency and renal dysfunction in the absence of skin manifestations: A variant of systemic sclerosis or a novel entity? Internal Medicine, 51(12), 1567–1572. https://doi.org/10.2169/internalmedicine.51.6924

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free