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1.
Malays J Pathol ; 41(1): 15-24, 2019 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-31025633

RESUMO

INTRODUCTION: In the event of encountering hydropic villi in products of conception specimens, pathologists will have to distinguish complete and partial hydatidiform mole (CHM & PHM) from hydropic abortion (HA). The histological diagnostic criteria are subjective and demonstrate considerable inter-observer variability. MATERIALS AND METHODS: This study evaluated the inter-observer variability in diagnosis of CHM, PHM and HA according to defined histologic criteria. Ninety abortus conception specimens were reviewed. Representative haematoxylin and eosin-stained slides were assigned independently to two pathologists who were asked to make a diagnosis of CHM, PHM or HA, and provide a report of the identified diagnostic histological criteria. Kappa value was calculated for the inter-observer agreement. RESULTS: There was a total of 36.7% disagreement between two pathologists (K = 0.403, Strength of Agreement = moderate), of which 24.4% and 12.2%, were differentiating PHM from CHM and PHM from HA, respectively. Among defined diagnostic histological criteria, the highest rate of agreement was observed in the identification of cistern formation and hydropic changes (K = 0.746 and 0.686 respectively, Strength of Agreement = substantial). CONCLUSION: There was moderate to substantial agreement rate between two pathologists in identification of two essential histologic criteria for diagnosis of molar pregnancies i.e. "hydropic change" and "trophoblastic proliferation".


Assuntos
Mola Hidatiforme/diagnóstico , Mola Hidatiforme/patologia , Neoplasias Uterinas/diagnóstico , Neoplasias Uterinas/patologia , Aborto Espontâneo/diagnóstico , Aborto Espontâneo/patologia , Diagnóstico Diferencial , Feminino , Humanos , Variações Dependentes do Observador , Gravidez
2.
Malays J Pathol ; 39(2): 201-205, 2017 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-28866706

RESUMO

Liposarcoma is regarded as the second most common soft tissue malignant tumour. Metastasis of liposarcoma to the heart is very rare, and to date, less than 40 cases have been reported in the literature. We report a 46 year-old male with myxoid liposarcoma of the lower extremity who developed extensive metastasis to the left ventricle, pulmonary artery, and pericardium. The patient presented with acute symptoms of dyspnea 16 years after surgical resection of the primary tumour, and his dyspnea progressed to cardio-respiratory arrest within the first few days of hospital admission.


Assuntos
Neoplasias Cardíacas/secundário , Lipossarcoma Mixoide/secundário , Pericárdio/patologia , Artéria Pulmonar/patologia , Neoplasias de Tecidos Moles/patologia , Evolução Fatal , Ventrículos do Coração/patologia , Humanos , Masculino , Pessoa de Meia-Idade
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