Panhypopituitarism without Thrombosis due to Primary Antiphospholipid Syndrome

被引：0

作者：

Gupta, Pulin Kumar ^{[1
]}

Mahto, Subodh Kumar ^{[1
]}

Balakrishna, Arjun Malasandra ^{[2
]}

Rampal, Parikha ^{[3
]}

Sharma, Narendra Kumar ^{[1
]}

机构：

[1] Dr RML Hosp, PGIMER, Dept Med, OPD Block, New Delhi 110001, India

[2] Sucheta Kriplani Hosp & LHMC, Dept Med, New Delhi, India

[3] Dr RML Hosp, PGIMER, Dept Radiol, New Delhi, India

来源：

JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH | 2019年 / 13卷 / 02期

关键词：

Autoimmune; Hormone replacement; Hypopituitarism;

D O I：

10.7860/JCDR/2019/40113.12566

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Hypopituitarism is a clinical syndrome in which pituitary hormones deficiency is seen in many conditions. Antiphospholipid Syndrome (APS) is an autoimmune disease characterised by antiphospholipid antibodies, commonly manifests as venous or arterial thrombosis with recurrent foetal loss. We here by report a case of 40-year-old female who presented with bilateral swelling of lower limbs with exertional breathlessness along with feeling of cold extremities, easy fatigability, lethargy and decreased appetite for six months which turned out to be hypopituitarism with APS. Hormone replacement was started and she experienced a good clinical improvement.

引用

页数：2

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