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1.
Acta Cytol ; 62(2): 145-150, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29275417

RESUMO

BACKGROUND: Follicular dendritic cell sarcoma (FDCS) is a rare neoplasm arising from follicular dendritic cells of germinal centers. The most common site of origin is lymph nodes and it may mimic a variety of tumors at that location, including carcinomas and sarcomas. Diagnosis is frequently missed on cytology as there are very few case reports describing the cytological characteristics of the lesion. Even on histology, a high degree of suspicion is required for an appropriate diagnosis. CASE: A 60-year-old male presented with a gradually increasing left submandibular mass that had been present for 3 months. Fine-needle aspiration cytology (FNAC) was performed, showing many clusters as well as scattered epithelioid cells with spindled to oval nuclei, nuclear pleomorphism, grooves, inclusions, and uniformly dispersed mature lymphocytes throughout the smears. The diagnosis of FDCS was suspected and was confirmed on histopathology and immunohistochemistry. CONCLUSION: FNAC can be a cheap, easy, and helpful tool in obtaining a diagnosis of FDCS as there are few characteristic cytological features that are better recognized than histology.


Assuntos
Sarcoma de Células Dendríticas Foliculares/patologia , Linfonodos/patologia , Biomarcadores Tumorais/análise , Biópsia por Agulha Fina , Sarcoma de Células Dendríticas Foliculares/metabolismo , Sarcoma de Células Dendríticas Foliculares/cirurgia , Diagnóstico Diferencial , Humanos , Imuno-Histoquímica , Linfonodos/química , Linfonodos/cirurgia , Masculino , Pessoa de Meia-Idade , Esvaziamento Cervical , Valor Preditivo dos Testes
2.
J Clin Diagn Res ; 11(4): ED03-ED04, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-28571151

RESUMO

Leiomyosarcomas (LMS) arising from vascular channel are rare and more often arise from inferior vena cava and pulmonary arteries. Primary renal vein LMS are even rarer and occur predominantly in females with peak in fifth and sixth decade. Preoperative diagnosis is difficult because these are rare tumours and present with symptoms and radiological findings similar to Renal Cell Carcinoma (RCC). We report a case of 55-year-old female who presented with abdominal discomfort with radiology showing a renal mass with features of RCC, radical nephrectomy was done and resected tumour showed an attachment to the wall of renal vein with morphology resembling LMS.

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