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. 2022 Jul;481(1):63-72.
doi: 10.1007/s00428-022-03332-5. Epub 2022 May 6.

Acellular mucin in lymph nodes isolated from treatment-naïve colorectal cancer resections: a clinicopathologic analysis of 16 cases

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Acellular mucin in lymph nodes isolated from treatment-naïve colorectal cancer resections: a clinicopathologic analysis of 16 cases

James E Lapinski et al. Virchows Arch. 2022 Jul.

Abstract

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.

Keywords: Acellular mucin; Colon cancer; Lymph nodes; Untreated.

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Conflict of interest statement

DECLARATIONS:

Conflict of interest: Alok A. Khorana, M.D. - Receives Institutional grant support from NIH, CDC, Leap, BMS, Celgene, Merck; Consulting fees from Janssen, Bayer, Pfizer, Anthos, Sanofi, BMS, Seagen, honorarium from Medscape for CME events, Support for attending meetings and/or travel from Janssen, Bayer, Seagen, BMS; Participated on a Data

Safety Monitoring Board or Advisory Board - Bayer, BMS, Janssen; Medical and Scientific Advisory Board, NBCA (unpaid).

All remaining authors have no conflicts of interest.

Figures

Figure 1:
Figure 1:
Acellular mucin deposit within a pericolonic lymph node from a 66-year-old woman with invasive moderately differentiated adenocarcinoma involving the ascending colon (pT3). (20X magnification)
Figure 2:
Figure 2:
Kaplan-Meier curve comparing survival outcomes shows that the clinical outcome of patients with acellular mucin (cases; study group) was more similar to pN0 controls compared to pN+ (N1) colon cancer controls.

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