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Diagnosis of thoracic SMARCA4-deficient undifferentiated tumor in cytology.
Kezlarian, Brie; Montecalvo, Joseph; Bodd, Francis M; Chang, Jason C; Riedel, Elyn; White, Charlie; Rekhtman, Natasha; Sauter, Jennifer L.
Afiliación
  • Kezlarian B; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Montecalvo J; Department of Pathology, Henry Ford Hospital, Detroit, MI, USA.
  • Bodd FM; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Chang JC; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Riedel E; Department of Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • White C; Department of Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Rekhtman N; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Sauter JL; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Cancer Cytopathol ; 131(8): 526-534, 2023 08.
Article en En | MEDLINE | ID: mdl-37278102
ABSTRACT

INTRODUCTION:

Although alterations in SMARCA4-deficient occur in non-small cell lung carcinoma (SD-NSCLC), thoracic SMARCA4-deficient undifferentiated tumor (TSDUT) is recognized as a distinct entity in the 2021 World Health Organization Classification of Thoracic Tumors because of unique morphologic, immunophenotypic and molecular features, and worse survival compared with SD-NSCLC. Cytologic diagnosis of TSDUT is clinically important because of its aggressive behavior and because it is often diagnosed by fine-needle aspiration because TSDUTs are usually unresectable at presentation. Here, we identify cytologic features that can be used for recognition of TSDUT and distinction from SD-NSCLC. MATERIALS AND

METHODS:

Cytomorphologic features were investigated in cytology specimens from patients with TSDUT (n = 11) and compared with a control group of patients with SD-NSCLC (n = 20).

RESULTS:

The presence of classic rhabdoid morphology, at least focally, was entirely specific for TSDUT (n = 6, 55%) compared with SD-NSCLC (n = 0) in this study. TSDUT more frequently showed tumor necrosis (n = 11, 100% vs. n = 8, 40%; p = .001), dominant single-cell pattern on aspirate smears or touch preparation slides (n = 8 [of 9], 80% vs. n = 3, 15%; p = .010), nuclear molding (n = 5, 45% vs. n = 1, 5%; p = .013), and indistinct cell borders (n = 11, 100% vs. n = 5, 25%; P < .001) compared with SD-NSCLC, respectively.

CONCLUSIONS:

Cytomorphologic features occurring more frequently in TSDUT include tumor necrosis, dominant single-cell pattern, nuclear molding indistinct cell borders, and focal rhabdoid cells. Presence of these features in a cytology specimen of an undifferentiated tumor, particularly in a patient with a thoracic mass, should raise suspicion for TSDUT and prompt appropriate ancillary workup.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Torácicas / Carcinoma de Pulmón de Células no Pequeñas / Carcinoma Pulmonar de Células Pequeñas / Neoplasias Pulmonares Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Cytopathol Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Torácicas / Carcinoma de Pulmón de Células no Pequeñas / Carcinoma Pulmonar de Células Pequeñas / Neoplasias Pulmonares Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Cytopathol Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos