Type I Dyserythropoietic Anemia in an Elderly Patient

نویسندگان

  • Jorge E. Maldonado
  • Howard F. Taswell
چکیده

A woman born in September 1912 was examined at the Mayo Clinic in March 1971. She had a history of chronic anxiety state and functional fatigue. For at least 35 yr she had been mildly anemic, and various treatments given elsewhere, including iron, liver extract, and vitamin B,2, had not helped her. Fifteen years before her present admission she had had a bone marrow study that was interpreted as “suggestive of pernicious anemia.” The family history was negative for blood dyscrasias. A cholecystectomy had been performed in 1955 for cholelithiasis; she was not jaundiced. Her breasts had been removed, one 15 and one 18 yr before, because of cancer; no recurrences were noted. Results of the physical examination were not remarkable, except for atrial fibrillation. The spleen and liver were not palpable. The hemoglobin level was 10.8 g/dl; erythrocyte count was 3,010,000/cu mm, and leukocyte count was 6400 cu/mm, with a normal differential count. The platelet count was 216,000 cu/mm, and the reticubocyte count was 2.1%. Marked anisopoikibocytosis, with significant oval macrocytosis and prominent basophilic stippling, was seen on a peripheral blood smear. Free gastric hydrochloric acid was present. The serum levels of vitamin B,2 and folate were normal. The serum iron level was 117 g/d1, and the total iron-binding capacity was 169 g/dl, with 69#{176},, saturation. Between 1971 and December 1973, the patient did well, and the hemoglobin level has remained stable.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A case of congenital dyserythropoietic anemia type IV

Congenital dyserythropoietic anemias (CDAs) are displayed by ineffective erythropoiesis. The wide variety of phenotypes observed in CDA patients makes differential diagnosis difficult; identification of the genetic variants is crucial in clinical management. We report the fifth case of a patient with unclassified CDAs, after genetic study, with CDA type IV.

متن کامل

Hereditary hemochromatosis in a patient with congenital dyserythropoietic anemia.

Herein is described the case of a young woman presenting with iron overload and macrocytosis. The initial diagnosis was hereditary hemochromatosis. Severe anemia developed after a few phlebotomies, and she was also found to have congenital dyserythropoietic anemia that, though not completely typical, resembled type II. Only genetic testing allowed the definition of the coexistence of the 2 dise...

متن کامل

Brief report Hereditary hemochromatosis in a patient with congenital dyserythropoietic anemia

Herein is described the case of a young woman presenting with iron overload and macrocytosis. The initial diagnosis was hereditary hemochromatosis. Severe anemia developed after a few phlebotomies, and she was also found to have congenital dyserythropoietic anemia that, though not completely typical, resembled type II. Only genetic testing allowed the definition of the coexistence of the 2 dise...

متن کامل

Acute Liver Failure in a Pediatric Patient with Congenital Dysery-Thropoietic Anemia Type I Treated with Deferasirox

Congenital dyserythropoietic anemias (CDA) represent a heterogeneous group of disorders characterized by morphological abnormalities of erythroid precursor cells and various degrees of hemolysis. Iron overload is a result of continuous hemolysis and recurrent transfusions. It is treated with iron chelators, including deferasirox. We present here a case of acute liver failure in a 12 years old g...

متن کامل

Congenital erythropoietic porphyria, diminished activity of uroporphyrinogen decarboxylase and dyserythropoiesis.

A 51 -yr-old white male with congenital erythropoietic porphyria (Gunther’s Disease) is described. The disease was first manifested in infancy and mutilating cutaneous photosensitivity eventually developed. The source of excess porphyrin production was a markedly dyserythropoietic bone marrow. The dyserythropoietic changes were most marked in the orthochromic and polychromatophilic normoblasts....

متن کامل

Glycophorin A in two patients with congenital dyserythropoietic anemia type I and type II is partly unglycosylated.

Glycophorins A from erythrocyte membranes of two patients with congenital dyserythropoietic anemia type I and type II (CDA type I and II) were analyzed for carbohydrate molar composition employing a modification of the recently published method that allowed simultaneous determination of carbohydrates and protein in electrophoretic bands of glycoproteins separated by sodium dodecyl sulfate-polya...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2005