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2.
Rev Esp Patol ; 55 Suppl 1: S32-S38, 2022 09.
Artigo em Espanhol | MEDLINE | ID: mdl-36075660

RESUMO

Deciduoid mesothelioma is an uncommon histological variant of epithelial mesothelioma which is extremely clinically aggressive. We report 3 cases of pleural caducoid mesothelioma in women of 75, 74 and 23 years of age. All patients presented with dyspnoea, vomiting and pelvic pain. Their imaging studies showed nodular pleuropericardic thickening, a parietal pleuropericardic solid mass and a large thoracic mass, respectively. Only one of them could be treated with chemotherapy, surgery and radiotherapy. Post diagnostic survival was 24 days, 1 month and 17 months respectively (mean 6.2 months). We describe the clinicopathological and immunohistochemical findings together with a review of the relevant literature.


Assuntos
Mesotelioma , Neoplasias Pleurais , Diagnóstico por Imagem , Feminino , Humanos , Mesotelioma/diagnóstico , Mesotelioma/patologia , Neoplasias Pleurais/diagnóstico , Neoplasias Pleurais/patologia
3.
Rev Esp Patol ; 54(2): 132-135, 2021.
Artigo em Espanhol | MEDLINE | ID: mdl-33726890

RESUMO

Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia is an infrequent lesion recently classified by the WHO as preinvasive. It can present with the formation of tumorlets (neuroendocrine cell groups up to 5 mm) which result in a typical histological and radiological image. We report a case of a 67-year-old women who presented with a chronic cough. The CT scan showed bilateral minute, multiple pulmonary nodules. A biopsy revealed a diffuse idiopathic pulmonary neuroendocrine cell hyperplasia with several tumorlets. After two years of follow-up, imaging studies showed no significant changes.


Assuntos
Pulmão/patologia , Células Neuroendócrinas/patologia , Idoso , Biópsia , Calcitonina/análise , Cromograninas/análise , Doença Crônica , Tosse , Feminino , Humanos , Hiperplasia/diagnóstico por imagem , Hiperplasia/patologia , Pulmão/química , Pulmão/diagnóstico por imagem , Células Neuroendócrinas/química , Tomografia Computadorizada por Raios X
4.
Rev Esp Patol ; 54(2): 141-144, 2021.
Artigo em Espanhol | MEDLINE | ID: mdl-33726892

RESUMO

Genital filariasis is an uncommon infectious entity in the western world. It has characteristic clinical features and a well-recognized endemic area that causes typical histological alterations. We report a case of a 32-year-old woman, a native of Mozambique, who presented with vulvar elephantiasis as a pendulous tumor with a maximum diameter of 15cm. A large part of the genital mass was resected. Microscopically, hyperkeratosis with irregular acanthosis, a notable thickening of dermis with dense fibrosis and inflammatory clusters of patchy distribution, mostly made up of plasma cells, was seen. Since the parasite was not observed, an exclusion diagnosis was made, as frequently happens with this lesion.


Assuntos
Filariose Linfática/patologia , Doenças da Vulva/patologia , Adulto , Filariose Linfática/cirurgia , Feminino , Humanos , Fotografação , Vulva/patologia , Vulva/cirurgia , Doenças da Vulva/cirurgia
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