Spontaneous Regression Of Bilateral Surrenal Haematoma And Subclinical Hypoaldosteronism In A Patient With Renal Amyloidosis Secondary To Familial Mediterranean Fever
Kara, & Paydaş, S. (2000). spontaneous regression of bilateral surrenal haematoma and subclinical hypoaldosteronism in a patient with renal amyloidosis secondary to Familial Mediterranean Fever. International urology and nephrology, 32(2), 291–292. https://doi.org/10.1023/a:1007196926394
View Original Source →Abstract
This report describes a patient with Familial Mediterranean Fever (FMF) associated with renal amyloidosis, bilaretal surrenal haematomas and hypoaldosteronism which was clinically asymptomatic. The deposition of AA amyloide was found on the renal and bone marrow biopsies. Bilateral surrenal haematoma regressed after six month from the first events. Colchicine therapy controlled the attacks of the disease.
Case Details
Disease Location
Kidney/adrenal glands bilateral
Personal Characteristics
38 years old woman. Operated of appendicitis at the age of 5. At 26 right oophorectomy. At 37 ovarian cystectomy. Patient had smoked one pack of cigarettes daily for 20 years.
Clinical Characteristics
Nausea, vomiting and abdominal pain. 10 years suffering from periodic abdominal and fever attacks. Familial mediterrean fever diagnosed.
Remission Characteristics
After 6 months from the first admission her abdominal CT and usg revealed total regression of surreal haematoma.
Treatment & Mechanisms
Proposed Remission Mechanisms
Not discussed
Clinical Treatment
Colcihine 1 mg/day