Dysplasia and carcinoma of the gallbladder: pathological evaluation, sampling, differential diagnosis and clinical implications
- PMID: 33629395
- DOI: 10.1111/his.14360
Dysplasia and carcinoma of the gallbladder: pathological evaluation, sampling, differential diagnosis and clinical implications
Abstract
Pathological evaluation of gallbladder neoplasia remains a challenge. A significant proportion of cases presents as clinically and grossly inapparent lesions, and grossing protocols are not well established. Among epithelial alterations, pseudo-pyloric gland metaplasia is ubiquitous and of no apparent consequence, whereas goblet cell metaplasia and a foveolar change in surface cells require closer attention. Low-grade dysplasia is difficult to objectively define and appears to be clinically inconsequential by itself; however, extra sampling is required to exclude the possibility of accompanying more significant lesions. For high-grade dysplasia ('high-grade BilIN', also known as 'carcinoma in situ'), a complete sampling is necessary to rule out invasion. Designating in-situ or minimally invasive carcinomas limited to muscularis or above as early gallbladder carcinoma (EGBC) helps to alleviate the major geographical differences (West/East) in the criteria for 'invasiveness' to assign a case to pTis or pT1. Total sampling is crucial in proper diagnosis of such cases. A subset of invasive GBCs (5-10%) arise from the intracholecystic neoplasm (ICN, 'adenoma-carcinoma sequence') category. Approximately two-thirds of ICNs have invasive carcinoma. However, this propensity differs by subtype. True 'pyloric gland adenomas' (> 1 cm) are uncommon and scarcely associated with invasive carcinoma. A distinct subtype of ICN composed of tubular, non-mucinous MUC6+ glands [intracholecystic tubular non-mucinous neoplasm (ICTN)] forms a localised pedunculated polyp. Although it is morphologically complex and high-grade, it appears to be invasion-resistant. Some of the invasive carcinoma types in the gallbladder have been better characterised recently with adenosquamous, neuroendocrine, poorly cohesive and mucinous carcinomas often being more advanced and aggressive.
Keywords: dysplasia; gallbladder carcinoma; gallbladder neoplasms; pathological evaluation.
© 2021 John Wiley & Sons Ltd.
References
-
- Bertran E, Heise K, Andia ME, Ferreccio C. Gallbladder cancer: incidence and survival in a high-risk area of Chile. Int. J. Cancer 2010; 127; 2446-2454.
-
- Roa J, Adsay NV, Arola J, Tsu W, Zen Y. Carcinoma of the gallbladder. In Board E ed. Digestive system tumours. WHO classification of tumours. 1. 5th ed. Lyon: IARC, 2019; 283-288.
-
- Mazer LM, Losada HF, Chaudhry RM et al. Tumor characteristics and survival analysis of incidental versus suspected gallbladder carcinoma. J. Gastrointest. Surg. 2012; 16; 1311-1317.
-
- Roa JC, Tapia O, Manterola C et al. Early gallbladder carcinoma has a favorable outcome but Rokitansky-Aschoff sinus involvement is an adverse prognostic factor. Virchows Arch. 2013; 463; 651-661.
-
- Roa JC, Adsay NV, Arola J, Tsu WM, Zen Y. Carcinoma of the gallbladder. In Klimstra DS, Lam AK, Paradis V, Schirmacher P eds. WHO classification of tumours of the digestive system. 5th ed. Lyon: IARC, 2019; 283-288.
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