A. Goldenberg et Sr. Tollin, MASSIVE BILATERAL ADRENAL HEMORRHAGE AND ADRENAL CRISIS IN 2 PATIENTSWITH THE PRIMARY ANTIPHOSPHOLIPID SYNDROME, The Endocrinologist, 8(5), 1998, pp. 365-368
A small number of cases of patients with the primary antiphospholipid
(APL) syndrome who developed massive bilateral adrenal hemorrhage have
been described. We describe two additional cases of patients with the
primary APL syndrome who developed massive bilateral adrenal hemorrha
ge. Case 1: A 68 year-old man who previously was diagnosed with the pr
imary APL syndrome sustained a myocardial infarction associated with a
lower gastrointestinal hemorrhage. He was maintained on warfarin ther
apy. Computed tomography (CT) of the abdomen revealed bilateral adrena
l hemorrhage. The patient subsequently developed an adrenal crisis. Ca
se 2: A previously healthy 39-year-old man presented with right-sided
abdominal pain. He was discovered to have a right renal infarction, an
d intravenous heparin therapy was begun. Within 48 hours he developed
an adrenal crisis. An abdominal CT scan confirmed bilateral adrenal he
morrhage. The patient ultimately was found to have a low titer of immu
noglobulin M anticardiolipin antibodies. Con elusion: Massive bilatera
l adrenal hemorrhage can complicate the primary APL syndrome. Patients
who develop unexplained bilateral adrenal hemorrhage should be tested
for the primary APL syndrome because it may be an early manifestation
of the disease.