Japanese Journal of Clinical Oncology, Vol 28, Issue 11 696-701, Copyright © 1998 by Foundation for Promotion of Cancer Research
S Mizobuchi, T Yamashiro, Y Nonami, A Yamamoto, M Kume, H Nakaya, T Sawada, H Taguchi, T Moriki and S Ogoshi
A case of pure red cell aplasia (PRCA), myasthenia gravis (MG) and thymoma
is reported. A 70-year-old woman presented with severe anemia. She had been
diagnosed as having MG 8 years earlier and her symptoms were adequately
controlled with ambenonium chloride. When she visited our hospital, her
hematocrit was 13.7% with a hemoglobin concentration of 4.7 g/dl and her
reticulocyte counts were persistently abnormal at 0.1%. Although both
direct and indirect Coombs' tests were positive, there was no evidence of
hemolysis. Routine screening tests for other etiologies of anemia were
negative. Serological tests for anti-DNA and anti-acetylcholine receptor
antibodies gave positive results. A bone marrow examination revealed severe
erythroid hypoplasia. PRCA was diagnosed and the patient was treated with
periodic transfusions. A lateral view chest roentgenogram and a computed
tomography scan of the thorax showed the presence of an anterior
mediastinal mass which was suspected to be thymoma. The patient underwent
thymothymectomy and the tumor was diagnosed as a thymoma. Although the
patient received no treatment for MG and PRCA after surgery, her
hematological test results rapidly improved and she was discharged from the
hospital on the 29th postoperative day. At that time, her hematocrit was
33.2%, her hemoglobin concentration was 10.0 g/dl, her peripheral
reticulocyte level was 1.8% and her left partial ptosis had improved. She
is doing well, 9 months after surgery. For a patient to remain in remission
without treatment for PRCA and MG after thymothymectomy is extremely rare.
ORIGINAL ARTICLE
Pure red cell aplasia and myasthenia gravis with thymoma: a case report and review of the literature
Department of Surgery II, Kochi Medical School, Japan. vyg10377@niftyserve.or.jp
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