• Eukene Gainza, Sara Fernández, Daniel Martínez, Pedro Castro, Xavier Bosch, José Ramírez, Arturo Pereira, María T Cibeira, Jordi Esteve, and Josep M Nicolás.
• From the Hematology Department (EG, MTC, JE); Medical Intensive Care Unit (SF, PC, JMN); Pathology Department (DM, JR); Internal Medicine Department (XB); and Hemotherapy-Hemostasis Department (AP), Hospital Clinic, Barcelona, Spain.
• Medicine (Baltimore). 2014 Nov 1; 93 (24): 359363359-363.

AbstractPulmonary tumor thrombotic microangiopathy (PTTM) is a rare clinical entity where tumor cell embolisms in pulmonary circulation induce thrombotic microangiopathy (TMA), respiratory failure, and subacute cor pulmonale.We describe 3 cases of PTTM that presented as the initial manifestation of metastatic gastric adenocarcinoma with TMA and pulmonary infiltrates.All 3 cases had similar clinical and laboratory features, which included moderate thrombocytopenia without renal failure, hemolysis with extremely high serum lactate dehydrogenase levels, leukoerythroblastosis in peripheral blood smear, altered coagulation tests, lymphadenopathies, and interstitial pulmonary infiltrates. All patients died within 2 weeks of diagnosis. Two cases were initially misdiagnosed as idiopathic thrombotic thrombocytopenic purpura and treated with plasma exchange with no response. One patient had bone marrow infiltration by malignant cells. Autopsies revealed PTTM associated with gastric disseminated adenocarcinoma (signet-ring cell type in 2 patients and poorly differentiated type in 1).PTTM should be considered in the differential diagnosis of patients with fulminant microangiopathic hemolytic anemia, such as atypical thrombotic thrombocytopenic purpura, mainly those with pulmonary infiltrates, disseminated intravascular coagulation, or Trousseau syndrome.

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