Assuntos
Circulação Coronária , Anomalias dos Vasos Coronários/fisiopatologia , Neoplasias Primárias Desconhecidas/fisiopatologia , Tumores Neuroendócrinos/fisiopatologia , Tumores Neuroendócrinos/secundário , Fístula Vascular/fisiopatologia , Idoso , Angiografia Coronária , Anomalias dos Vasos Coronários/diagnóstico por imagem , Feminino , Ventrículos do Coração/fisiopatologia , Humanos , Neoplasias Hepáticas/fisiopatologia , Neoplasias Hepáticas/secundárioRESUMO
Lymphomas belong to the most treatable and curable malignant tumors of childhood. They should always be considered among differential diagnosis, even in unusual locations, and tumor material should be processed adequately to reach true diagnosis. The authors report on a 16-year-old adolescent with a tracheal lymphoma, a rare location of lymphoma in childhood. Because only formalin-fixed tumor material was obtained, pathology showed two differential diagnoses and the entity could never be fully clarified as anaplastic plasmacytoma or plasmoblastic lymphoma. Thus, full lymphoma diagnostic workup should be performed even in tumors with atypical location.
Assuntos
Linfoma de Células B/diagnóstico , Neoplasias da Traqueia/diagnóstico , Adolescente , Asma/diagnóstico , Diagnóstico Diferencial , Erros de Diagnóstico , Humanos , Linfoma de Células B/tratamento farmacológico , Masculino , Neoplasias da Traqueia/tratamento farmacológicoRESUMO
The HMGA2 gene has been found to be rearranged in a variety of benign solid tumors. However, in all tumor entities where aberrations of the corresponding chromosomal region have been found, a large percentage of tumors do not show any detectable cytogenetic deviation. Thus, the question arises whether or not in some of these cases, small subpopulations of tumor cells characterized by HMGA2 rearrangements exist. The existence of these populations would strongly suggest a secondary nature of the chromosomal aberrations. Herein, we have addressed this question by RT-PCR analyses of the HMGA2-LPP fusion resulting from t(3;12)(q27 approximately q28;q14 approximately q15) in a series of 61 pulmonary chondroid hamartomas (PCH) with an apparently normal karyotype. As a result, the HMGA2-LPP fusion transcript was amplified in only one of 61 PCH with a normal karyotype. In this case, fluorescence in situ hybridization analysis revealed a hidden chromosomal aberration. The absence of the HMGA2-LPP fusion in small populations of tumors with a normal karyotype suggests the primary nature of chromosomal rearrangements in the development of PCH affected by those aberrations.