Myelodysplastic syndrome and pancytopenia responding to treatment of hyperthyroidism: peripheral blood and bone marrow analysis before and after antihormonal treatment.
J Cancer Res Ther
; 2007 Jan-Mar; 3(1): 43-6
Article
en En
| IMSEAR
| ID: sea-111569
ABSTRACT
Hematological disorders, especially single lineage abnormalities, have been described in hyperthyroidism. Pancytopenia has been reported, without myelodysplastic syndrome or megaloblastic anemia. We studied the peripheral blood smear and the bone marrow aspiration and biopsy of a 65-year-old lady, who presented with pancytopenia and thyrotoxicosis due to multinodular goiter. She denied ingesting any toxic medication. At diagnosis WBC 2500/ul, platelets count 58,000/ul, hemoglobin level 6.5 g/dl. The bone marrow was moderately hyper cellular with moderate myelofibrosis and arrested hematopoiesis. The TSH level was 0.02 mIU/l (N 0.25-4), the fT3 18 pmol/l (N 4-10), the routine serum immunologic tests were negative. After treatment with single agent neomercazole (carbimazole), complete recovery of the blood cell counts was obtained within one month. The bone marrow aspiration, performed three months after starting therapy, showed normal hematopoiesis. The thyroid function tests returned to normal and no autoimmune reaction was detected on routine serum testing. Persistent response was observed six months later under medical treatment. The patient has refused surgical treatment. Reversible myelodysplastic syndrome may also be part of the changes in blood picture of patients with hyperthyroidism, probably due to direct toxic mechanism.
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IMSEAR
Asunto principal:
Pancitopenia
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Antitiroideos
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Pruebas de Función de la Tiroides
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Recuento de Células Sanguíneas
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Médula Ósea
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Síndromes Mielodisplásicos
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Anciano
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Femenino
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Humanos
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Carbimazol
Idioma:
En
Revista:
J Cancer Res Ther
Asunto de la revista:
Neoplasms
/
Therapeutics
Año:
2007
Tipo del documento:
Article