Skip to content
Research Article Open access CC BY 4.0

Pseudo-hypoparathyroidism Coexistent with Systemic Sclerosis: A Rare Case Report

Fatma Avci Merdin, Alparslan Merdin, Ugur Karasu, Safiye Arik, Ali Berkant Avci, Hasan Altunbas

Journal of Advances in Medicine and Medical Research · pp. 1–4 · Published 25 Mar 2017

10.9734/BJMMR/2017/15775

Abstract

Background: Systemic sclerosis is a chronic autoimmune inflammatory disease with wide-spread fibrosis of the skin and internal organs. The hypoparathyroidism associated with systemic sclerosis is infrequent and rarely reported in literature. Case Report: A 48 year-old female patient applied to our clinic with headache, increasing pallor and bruising cold of the hands. Physical examination revealed sclerodactyly and hardening on the skin of forearms and face. Centromeric type anti-nuclear antibodies were detected in the serum, and the patient and was diagnosed with systemic sclerosis. The same woman had also been diagnosed as epilepsy and she had been subjected on anti-epileptic drug therapy for 14 years. We found that she had also hypocalcemia (4,6mg/dl). She was diagnosed as pseudohypoparathyroidism. Conclusions: Pseudo-hypoparathyroidism associated with systemic sclerosis is a very rare entity. And pseudo-hypoparathyroidism should also be kept in mind in autoimmune disorders.

Hypocalcemia pseudohypoparathyroidism systemic sclerosis

Cited by 0

No indexed citations yet.

Article metrics

Real usage data collected on this platform.

19

Page views

0

PDF downloads

2

Outbound clicks

0

Citations

Views over time

Views by country

Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".

Traffic sources

Referring site, by host.

Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.