Myasthenia gravis in a patient with chronic myeloid leukemia treated by busulfan.
نویسندگان
چکیده
P.M., a seventy year old Polish-born male clerk, was referred to the Hematology Clinic in September 1963. Examination in another medical service in 1961 had revealed moderate hepatosplenomegaly, a platelet count of 900,000 per cu.mm. with normal red and white blood cell counts, and megakaryocytic hyperplasia in bone marrow with excessive platelet production and hyperplasia of the white cell series with a shift to the left but without blast cells. The diagnosis of primary thrombocythemia was made, and the possibility of transformation to myeloid leukemia was raised, but no specffic treatment was prescribed. Examination in our clinic in 1963 revealed hepatosplenomegaly, the spleen being palpated 6 cm. and the liver 2 cm. below the costal margin, both firm and nontender. Several enlarged nontender lymph glands of diameter up to 2 cm. were palpated in the neck and the axillae. The hemoglobin was 12.6 Cm. per cent, RBC 4,000,000 per cu.mm., hematocrit 40 per cent, reticulocyte count 0.1 per cent, and WBC 10,000 per cu.mm. with polymorphonuclears 65 per cent, band forms 4 per cent, eosinophils 4 per cent, blast cells 3 per cent, lymphocytes 24 per cent. The platelet count was 1,000,000 per cu.mm., bleeding tinue 6 mm., clotting time 5 mm., clot retraction normal, ESR (Westergren) 13 mm. in the first hour and 20 mm. in the second. The serum B1., level was 1250 m tg per ml., urea 42 mg. per cent, uric acid 6.5 mg. per cent. LE cells were not found. A sternal bone marrow biopsy smear was similar to the examination in 1961, except for the presence of a few blast coils. Leukocyte alkaline phosphatase staining showed a zero score. The clinical and hematologic findings were considered consistent with chronic myeloid leukemia. The patient refused treatment. In September 1964, his hemoglobin was 12.6 Cm. per cent, WBC 16,500 per cu.mm., with a normal differential count. The platelet count was 300,000 per cu.mm. The spleen, liver, and lymph glands were essentially unchanged since the previous examination.
منابع مشابه
MYASTHENIA GRAVIS AND THYMECTOMY: A 10-YEAR STUDY IN SHIRAZ
A retrospective comparative study was performed on 54 patients treated medically or surgically (thymectomy) for myasthenia gravis (MG) from 1979- 1989 in three Shiraz University Hospitals. Each surgical patient was compared with a medical patient on the basis of age, sex, severity and duration of disease. Complete remission was noted in 3 out of 27 thymectomized patients but in none of the...
متن کاملDevelopment of Myasthenia Gravis in a Patient with Chronic Myeloid Leukemia during Treatment with Nilotinib
We report on a patient diagnosed with chronic myeloid leukemia (CML) who developed myasthenia gravis while on treatment with nilotinib. Autoimmune disease, including the development of myasthenia gravis, has been described in association with CML as well as the use of tyrosine kinase inhibitors. Second generation tyrosine kinase inhibitors are highly effective in the treatment of CML, although ...
متن کاملA case of chronic inflammatory demyelinating polyneuropathy presented with unilateral ptosis
Chronic Inflammatory Demyelinating Polyneuropathy is an autoimmune disease with progressive and relapsing courses. The main clinical presentations are diffuse deep tendon hyporeflexia or areflexia and symmetric proximal-distal muscles weakness. Myasthenia gravis is also an immune mediated disease with fluctuating ocular and bulbar symptoms and sometimes weakness. Although both myasthenia grav...
متن کامللوسمی میلوئید مزمن در کودکان و گزارش یک مورد
SUMMARY Chronic Myeloid Leukemia In Children And a Case – Report Dr. Roya Ejte mai , Assistant. professor, Gilan University of medical Sciences, Rasht . The case is a ten-years - old boy. During examinations for massive splenomegaly, his disease has been diagnosed chronic Myelogenous leukemia (CML), and also philadelphia chromosome was revealed during chromosomal analysis. The patient was t...
متن کاملA Case Report of Congenital Myasthenia Gravis Presenting With Respiratory Distress
Congenital Myasthenic Syndromes (CMS) are rare inherited disorders characterized by dysfunction of neuromuscular transmission at the neuromuscular junction. Most patients with congenital myasthenic syndromes present in the infancy. Major symptoms of affected individuals include weakness and fatigue during the first years of life. Patients may show hypotonia, facial weakness, swallowing difficul...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Blood
دوره 32 2 شماره
صفحات -
تاریخ انتشار 1968