C. Sakai et al., MALIGNANT PHEOCHROMOCYTOMA ACCOMPANIED BY MICROANGIOPATHIC HEMOLYTIC-ANEMIA - A CASE-REPORT, Japanese Journal of Clinical Oncology, 24(3), 1994, pp. 171-174
A 63-year-old woman was in hospital for persistent backache. Four mont
hs prior to admission she had been pointed out as having hypertension
for the first time. On admission, she had anemia (hemoglobin 7.0 g/dl)
with reticulocytosis, and a blood smear showed fragmented erythrocyte
s. A bone marrow aspirate disclosed erythroid hyperplasia and invasion
of cancer cells. The chest roentgenogram showed a coin-lesion of the
right lung and left pleural effusion. A diagnosis of microangiopathic
hemolytic anemia (MAHA) associated with carcinomatosis was made, but t
he primary site of the cancer was unknown. Respiratory failure develop
ed and the patient died a month later. Surprisingly, the autopsy revea
led a malignant pheochromocytoma arising from the right adrenal gland
with massive metastases to the lungs, liver, lymph nodes and systemic
bones, and also disseminated intravascular coagulation (DIC). The DIC
would probably account for the MAHA in this case. To our knowledge, th
is is the first reported case of malignant pheochromocytoma accompanie
d by MAHA.