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Cytopathologic features of clear cell papillary renal cell carcinoma: A recently described variant to be considered in the differential diagnosis of clear cell renal epithelial neoplasms.
Sayeed, Sadia; Lindsey, Kathryn G; Baras, Alexander S; Jackson, Christopher; Powers, Celeste N; Uram-Tuculescu, Cora; Smith, Steven C.
Afiliação
  • Sayeed S; Department of Pathology, Virginia Commonwealth University Health System, Richmond, Virginia.
  • Lindsey KG; Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina.
  • Baras AS; Department of Pathology, Johns Hopkins University, Baltimore, Maryland.
  • Jackson C; School of Medicine, Virginia Commonwealth University Health System, Richmond, Virginia.
  • Powers CN; Department of Pathology, Virginia Commonwealth University Health System, Richmond, Virginia.
  • Uram-Tuculescu C; Department of Pathology, Virginia Commonwealth University Health System, Richmond, Virginia.
  • Smith SC; Department of Pathology, Virginia Commonwealth University Health System, Richmond, Virginia.
Cancer Cytopathol ; 124(8): 565-72, 2016 Aug.
Article em En | MEDLINE | ID: mdl-27062008
ABSTRACT

BACKGROUND:

Clear cell papillary renal cell carcinoma (CCPRCC) is a distinctive variant of renal cell carcinoma that has been formally adopted by the new Word Health Organization classification. An emerging consensus has documented its particularly indolent course and emphasized its separation from conventional clear cell renal cell carcinoma (CCRCC) for treatment planning. CCPRCC features in cytologic preparations have not been studied.

METHODS:

This study retrospectively identified a series of CCPRCCs that had cytology samples before the histopathologic diagnosis and reviewed corresponding cytologic materials, including aspirate smears, cell block materials, touch preparations, and core biopsy samples. The identified clinicopathologic and cytologic features were tabulated.

RESULTS:

Five cases of CCPRCC with cytopathologic materials were identified from 4 women and 1 man aged 34 to 70 years (2 with end-stage renal disease), and the sampled lesions were 1.8 to 11.0 cm. The original cytopathologic diagnostic considerations ranged from atypical cyst-lining cells to angiomyolipoma to CCRCC and CCPRCC. The aspirate and touch preparation samples showed scant cellularity with scattered sheets and clusters of small, bland epithelial cells (much smaller than admixed renal tubular cells) with optically clear cytoplasm (lacking conspicuous cytoplasmic vacuolization) and small, grade 1 nuclei. The cell block materials and the core biopsy samples showed cyst walls with prominent myomatous stroma lined by low-grade epithelium with optically clear cytoplasm, inverse nuclear polarization, and a characteristic cytokeratin 7-positive/carbonic anhydrase IX-positive phenotype. Three cases were treated with resection, 1 case was treated with ablation, and 1 case was under surveillance.

CONCLUSIONS:

CCPRCC demonstrates recognizable cytomorphologic features and merits consideration in the cytologic differential diagnosis for kidney lesions. With increasing experience, more conservative management may be contemplated. Cancer Cytopathol 2016;124565-72. © 2016 American Cancer Society.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Papilar / Carcinoma de Células Renais / Biomarcadores Tumorais / Células Epiteliais / Neoplasias Renais Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Cytopathol Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Papilar / Carcinoma de Células Renais / Biomarcadores Tumorais / Células Epiteliais / Neoplasias Renais Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Cytopathol Ano de publicação: 2016 Tipo de documento: Article