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Acellular mucin in lymph nodes isolated from treatment-naïve colorectal cancer resections: a clinicopathologic analysis of 16 cases.
Lapinski, James E; Khorana, Alok A; Rybicki, Lisa; Firat, Canan; Lee, Hwajeong; Piotti, Kathryn; Lewis, Eugene H; McNamara, Michael; Deshpande, Vikram; Shia, Jinru; Patil, Deepa T.
Afiliación
  • Lapinski JE; Department of Anatomic Pathology, Cleveland Clinic, Cleveland, OH, USA.
  • Khorana AA; Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH, USA.
  • Rybicki L; Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Firat C; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
  • Lee H; Department of Pathology and Laboratory Medicine, Albany Medical Center, Albany, NY, USA.
  • Piotti K; Department of Pathology, Morristown Medical Center, Morristown, NJ, USA.
  • Lewis EH; Department of Pathology, St. Vincent's Medical Center, Bridgeport, CT, USA.
  • McNamara M; Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH, USA.
  • Deshpande V; Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
  • Shia J; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
  • Patil DT; Department of Anatomic Pathology, Cleveland Clinic, Cleveland, OH, USA. dtpatil@bwh.harvard.edu.
Virchows Arch ; 481(1): 63-72, 2022 Jul.
Article en En | MEDLINE | ID: mdl-35513610
Lymph nodes with acellular mucin harvested from treated colorectal cancers (CRC) are staged as pN0. However, there is variability among pathologists while reporting the pN stage when acellular mucin is found within nodes of untreated CRCs. While the UICC guidelines suggest staging them as pN1, the AJCC and CAP do not offer any recommendations. In order to characterize their clinicopathologic features and outcome, we compared 16 untreated CRCs (study group; mean age: 68 years) harboring nodes with acellular mucin with 34 pN0 and 25 pN1 untreated CRC controls. All tumors were unifocal; 12 (75%) were right-sided lesions. Most cases (75%) showed one node with acellular mucin (range: 1-3). MMR-deficient tumors were significantly more common in the study group (83%) compared to pN0 (33%; p = 0.006) and pN1 controls (8%; p < 0.001). The overall survival of study group patients was closer to pN0 compared to pN1 controls; however, this difference was not statistically significant. In conclusion, untreated CRC that harbor acellular mucin within lymph nodes commonly present as right-sided, MMR-deficient tumors in older women that show a non-mucinous phenotype. While the limited number of cases precludes us from making any formal recommendations about staging, we suggest that the finding of acellular mucin in a node should prompt evaluation of deeper levels (with or without cytokeratin immunohistochemistry) and submission of all pericolonic fat for additional lymph node harvest. Whether acellular mucin in nodes of untreated CRCs is related to the indolent biology of the disease, a robust local immune response or MMR deficiency requires further investigation.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Mucinas Tipo de estudio: Guideline Idioma: En Revista: Virchows Arch Asunto de la revista: BIOLOGIA MOLECULAR / PATOLOGIA Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Mucinas Tipo de estudio: Guideline Idioma: En Revista: Virchows Arch Asunto de la revista: BIOLOGIA MOLECULAR / PATOLOGIA Año: 2022 Tipo del documento: Article