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DOI 10.1016/j.transci.2009.10.010

Медицинская библиотека · Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis · 2009

Thrombotic thrombocytopenic purpura as the first manifestation of metastatic adenocarcinoma in a young woman.

Kadikoylu Gurhan, Barutca Sabri, Tataroglu Canten, Kafkas Samet, Erpek Hakan, Meydan Nezih, Yavasoglu Irfan, Bolaman Zahit

Клинический случайСтатьяПеревод в очереди

Аннотация

Thrombotic microangiopathy occurs in 5-10% of patients with mucin-producing disseminated adenocarcinoma. A 28-year-old woman complained of fatigue, bone pain, and weight loss. There were pallor, icterus, and tenderness in the bones on physical examination. Microangiopathic hemolytic anemia, leukoerythroblastic picture, thrombocytopenia, and normal coagulation tests were detected. Thrombotic thrombocytopenic purpura (TTP) was diagnosed and therapeutic plasma exchange was performed on the patient. On day 5 a laparotomy had to be performed because of acute abdomen due to the rupture of a corpus hemorrhagicum follicle of an ovary. Signet ring cell adenocarcinoma stained with cytokeratin 7 and mucicarmine was seen on ovaries and bone marrow, after the pathological examination. The primary site of tumor could not be investigated, because of the patient's refusal. Although chemotherapy including cis-platinum, infusional 5-fluorouracil, and calcium leucovorin were administered in two courses, she died from respiratory failure. In conclusion, malignancy and bone marrow involvement should be considered when associated with leukoerythroblastic picture and TTP.

Для цитирования: Kadikoylu Gurhan, Barutca Sabri, Tataroglu Canten, Kafkas Samet, Erpek Hakan, Meydan Nezih, Yavasoglu Irfan, Bolaman Zahit. Thrombotic thrombocytopenic purpura as the first manifestation of metastatic adenocarcinoma in a young woman.. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis. 2009. DOI: 10.1016/j.transci.2009.10.010.

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