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Concurrent Adjacent Merkel Cell Carcinoma and Chronic Lymphocytic Leukemia without Simultaneous Merkel Cell Polyomavirus Detection: A Case Series.
Saade, Rayan; Najjar, Saleh; Arslan, Mustafa Erdem; Rady, Peter; Tyring, Stephen K; Nazeer, Tipu.
Afiliación
  • Saade R; Department of Pathology and Laboratory Medicine, Albany Medical Center, Albany, NY 12208, USA.
  • Najjar S; Department of Pathology and Laboratory Medicine, Albany Medical Center, Albany, NY 12208, USA.
  • Arslan ME; Department of Pathology and Laboratory Medicine, Albany Medical Center, Albany, NY 12208, USA.
  • Rady P; Department of Dermatology, McGovern Medical School, University of Texas Health Science Center, Houston, TX 77004, USA.
  • Tyring SK; Department of Dermatology, McGovern Medical School, University of Texas Health Science Center, Houston, TX 77004, USA.
  • Nazeer T; Department of Pathology and Laboratory Medicine, Albany Medical Center, Albany, NY 12208, USA.
Dermatopathology (Basel) ; 8(2): 190-201, 2021 Jun 07.
Article en En | MEDLINE | ID: mdl-34200164
BACKGROUND: The association between Merkel cell carcinoma (MCC) and chronic lymphocytic leukemia/small lymphocytic leukemia (CLL/SLL) is well established in the literature. A majority of MCCs are known to be associated with Merkel cell carcinoma polyomavirus (MCPyV), which is postulated to be a possible causative agent linking these two entities. We aim to identify the presence of MCPyV in patients with concurrent adjacent MCC and CLL/SLL. METHODS: Archived pathology materials of three cutaneous or surgical excisions with concurrent MCC and CLL/SLL were reviewed. Additional 12-µm sections from paraffin-embedded tissue of these resections were matched with original hematoxylin and eosin-stained slides and used to extract foci from each tumor separately. DNA was extracted from these tissues, and polymerase chain reaction (PCR), utilizing a primer set within a highly conserved "small T" viral DNA region, was done to detect MCPyV. RESULTS: Out of 140 cases of cutaneous or surgical excisions with MCC identified in our electronic medical records (EMR), three had coexisting neighboring CLL/SLL in the same resection specimen. In one case out of three, MCPyV was detected in MCC but not in CLL/SLL. The remaining two cases showed no detection of MCPyV in either MCC or CLL/SLL. CONCLUSION: MCPyV was not concurrently associated with adjacent MCC and CLL/SLL, indicating that it is not driving simultaneous tumorigenesis, at least in a subset of these cases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 Problema de salud: 1_sistemas_informacao_saude Tipo de estudio: Diagnostic_studies Idioma: En Revista: Dermatopathology (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 Problema de salud: 1_sistemas_informacao_saude Tipo de estudio: Diagnostic_studies Idioma: En Revista: Dermatopathology (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
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