Hepatic Cysts: Reappraisal of the Classification, Terminology, Differential Diagnosis, and Clinicopathologic Characteristics in 258 Cases.


Journal

The American journal of surgical pathology
ISSN: 1532-0979
Titre abrégé: Am J Surg Pathol
Pays: United States
ID NLM: 7707904

Informations de publication

Date de publication:
01 09 2022
Historique:
pubmed: 3 7 2022
medline: 19 8 2022
entrez: 2 7 2022
Statut: ppublish

Résumé

The literature on liver cysts is highly conflicting, mostly owing to definitional variations. Two hundred and fifty-eight ≥1 cm cysts evaluated pathologically using updated criteria were classifiable as: I. Ductal plate malformation related (63%); that is, cystic bile duct hamartoma or not otherwise specified-type benign biliary cyst (35 with polycystic liver disease). These were female predominant (F/M=2.4), large (10 cm), often multifocal with degenerative/inflammatory changes and frequently misclassified as "hepatobiliary cystadenoma." II. Neoplastic (13%); 27 (10.5%) had ovarian-type stroma (OTS) and qualified as mucinous cystic neoplasm (MCN) per World Health Organization (WHO). These were female, solitary, mean age 52, mean size 11 cm, and 2 were associated with carcinoma (1 in situ and 1 microinvasive). There were 3 intraductal papillary neoplasms, 1 intraductal oncocytic papillary neoplasm, 1 cystic cholangiocarcinoma, and 2 cystic metastasis. III. Infectious/inflammatory (12%). These included 23 hydatid cysts (including 2 Echinococcus alveolaris both misdiagnosed preoperatively as cancer), nonspecific inflammatory cysts (abscesses, inflammatory cysts: 3.4%). IV. Congenital (7%). Mostly small (<3 cm); choledochal cyst (5%), foregut cyst (2%). V. Miscellaneous (4%). In conclusion, hepatic cysts occur predominantly in women (3/1), are mostly (90%) non-neoplastic, and seldom (<2%) malignant. Cystic bile duct hamartomas and their relative not otherwise specified-type benign biliary cysts are frequently multifocal and often misdiagnosed as "cystadenoma/carcinoma." Defined by OTS, MCNs (the true "hepatobiliary cystadenoma/carcinoma") are solitary, constitute only 10.5% of hepatic cysts, and have a significantly different profile than the impression in the literature in that essentially all are perimenopausal females, and rarely associated with carcinoma (7%). Since MCNs can only be diagnosed by demonstration of OTS through complete microscopic examination, it is advisable to avoid the term "cystadenoma/cystadenocarcinoma" solely based on radiologic examination, and the following simplified terminology would be preferable in preoperative evaluation to avoid conflicts with the final pathologic diagnosis: (1) noncomplex (favor benign), (2) complex (in 3 subsets, as favor benign, cannot rule out malignancy, or favor malignancy), (3) malignant features.

Identifiants

pubmed: 35778790
doi: 10.1097/PAS.0000000000001930
pii: 00000478-202209000-00005
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1219-1233

Informations de copyright

Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest and Source of Funding: The authors have disclosed that they have no significant relationships with, or financial interest in, any commercial companies pertaining to this article.

Références

Rawla P, Sunkara T, Muralidharan P, et al. An updated review of cystic hepatic lesions. Clin Exp Hepatol. 2019;5:22–29.
Mavilia MG, Pakala T, Molina M, et al. Differentiating cystic liver lesions: a review of imaging modalities, diagnosis and management. J Clin Transl Hepatol. 2018;6:208–216.
Kelly K, Weber SM. Cystic diseases of the liver and bile ducts. J Gastrointest Surg. 2014;18:627–634; quiz 634.
Arnaoutakis DJ, Kim Y, Pulitano C, et al. Management of biliary cystic tumors: a multi-institutional analysis of a rare liver tumor. Ann Surg. 2015;261:361–367.
Sang X, Sun Y, Mao Y, et al. Hepatobiliary cystadenomas and cystadenocarcinomas: a report of 33 cases. Liver Int. 2011;31:1337–1344.
Xu MY, Shi XJ, Wan T, et al. Clinicopathological characteristics and prognostic factors of intrahepatic biliary cystadenocarcinoma. Chin Med J (Engl). 2015;128:1177–1183.
Boyum JH, Sheedy SP, Graham RP, et al. Hepatic mucinous cystic neoplasm versus simple biliary cyst: assessment of distinguishing imaging features using CT and MRI. Am J Roentgenol. 2021;216:403–411.
Kubota K, Nakanuma Y, Kondo F, et al. Clinicopathological features and prognosis of mucin-producing bile duct tumor and mucinous cystic tumor of the liver: a multi-institutional study by the Japan Biliary Association. J Hepatobiliary Pancreat Sci. 2014;21:176–185.
Anderson MA, Dhami RS, Fadzen CM, et al. CT and MRI features differentiating mucinous cystic neoplasms of the liver from pathologically simple cysts. Clin Imaging. 2021;76:46–52.
Devaney K, Goodman ZD, Ishak KG. Hepatobiliary cystadenoma and cystadenocarcinoma. A light microscopic and immunohistochemical study of 70 patients. Am J Surg Pathol. 1994;18:1078–1091.
Nakajima T, Sugano I, Matsuzaki O, et al. Biliary cystadenocarcinoma of the liver. A clinicopathologic and histochemical evaluation of nine cases. Cancer. 1992;69:2426–2432.
Soares KC, Arnaoutakis DJ, Kamel I, et al. Cystic neoplasms of the liver: biliary cystadenoma and cystadenocarcinoma. J Am Coll Surg. 2014;218:119–128.
Kishida N, Shinoda M, Masugi Y, et al. Cystic tumor of the liver without ovarian-like stroma or bile duct communication: two case reports and a review of the literature. World J Surg Oncol. 2014;12:229–236.
Tran S, Berman L, Wadhwani NR, et al. Hepatobiliary cystadenoma: a rare pediatric tumor. Pediatr Surg Int. 2013;29:841–845.
Kazama S, Hiramatsu T, Kuriyama S, et al. Giant intrahepatic biliary cystadenoma in a male: a case report, immunohistopathological analysis, and review of the literature. Dig Dis Sci. 2005;50:1384–1389.
Quigley B, Reid MD, Pehlivanoglu B, et al. Hepatobiliary mucinous cystic neoplasms with ovarian type stroma (so-called “hepatobiliary cystadenoma/cystadenocarcinoma”): clinicopathologic analysis of 36 cases illustrates rarity of carcinomatous change. Am J Surg Pathol. 2018;42:95–102.
Compagno J, Oertel JE. Mucinous cystic neoplasms of the pancreas with overt and latent malignancy (cystadenocarcinoma and cystadenoma). A clinicopathologic study of 41 cases. Am J Clin Pathol. 1978;69:573–580.
Basturk O, Nakayuma Y, Aishima S, et al. World Health Organisation, International Agency for Research on Cancer. WHO Classification of the Digestive System Tumours; 2019.
Adsay NV, Kloeppel G, Fukushima N, et al. Intraductal neoplasms of the pancreas. In: Bosman FT, ed. WHO Classification of Tumors of the Digestive System , 4th ed. Lyon, France: International Agency for Research on Cancer; 2010:304–313.
Tanaka M, Fernandez-del Castillo C, Adsay V, et al. International consensus guidelines 2012 for the management of IPMN and MCN of the pancreas. Pancreatology. 2012;12:183–197.
Kloppel G, Adsay V, Konukiewitz B, et al. Precancerous lesions of the biliary tree. Best Pract Res Clin Gastroenterol. 2013;27:285–297.
Schlitter AM, Jang KT, Kloppel G, et al. Intraductal tubulopapillary neoplasms of the bile ducts: clinicopathologic, immunohistochemical, and molecular analysis of 20 cases. Mod Pathol. 2015;28:1249–1264.
Wang T, Askan G, Adsay V, et al. Intraductal oncocytic papillary neoplasms: clinical-pathologic characterization of 24 cases, with an emphasis on associated invasive carcinomas. Am J Surg Pathol. 2019;43:656–661.
Rouzbahman M, Serra S, Adsay NV, et al. Oncocytic papillary neoplasms of the biliary tract: a clinicopathological, mucin core and Wnt pathway protein analysis of four cases. Pathology. 2007;39:413–418.
Martin DR, Kalb B, Sarmiento JM, et al. Giant and complicated variants of cystic bile duct hamartomas of the liver: MRI findings and pathological correlations. J Magn Reson Imaging. 2010;31:903–911.
Zen Y, Terahata S, Miyayama S, et al. Multicystic biliary hamartoma: a hitherto undescribed lesion. Hum Pathol. 2006;37:339–344.
Tapper EB, Martin D, Adsay NV, et al. Symptomatic bile duct hamartomas: surgical management in an MRI driven practice. J Gastrointest Surg. 2010;14:1265–1270.
Awasthi A, Das A, Srinivasan R, et al. Morphological and immunohistochemical analysis of ductal plate malformation: correlation with fetal liver. Histopathology. 2004;45:260–267.
Brunetti E, Kern P, Vuitton DA, et al. Expert consensus for the diagnosis and treatment of cystic and alveolar echinococcosis in humans. Acta Trop. 2010;114:1–16.
Wittekind CFHP, Ponchon T. Bile Duct Cystadenoma and Cystadenocarcinoma World Health Organization, Pathology and Genetics of Tumors of the Digestive System, 3th ed. Lyon, France: International Agency for Research on Cancer; 2000:182–183.
Zhelnin K, Xue Y, Quigley B, et al. Nonmucinous biliary epithelium is a frequent finding and is often the predominant epithelial type in mucinous cystic neoplasms of the pancreas and liver. Am J Surg Pathol. 2017;41:116–120.
Jang KT, Park SM, Basturk O, et al. Clinicopathologic characteristics of 29 invasive carcinomas arising in 178 pancreatic mucinous cystic neoplasms with ovarian-type stroma: implications for management and prognosis. Am J Surg Pathol. 2015;39:179–187.
Zen Y, Jang KT, Ahn S, et al. Intraductal papillary neoplasms and mucinous cystic neoplasms of the hepatobiliary system: demographic differences between Asian and Western populations, and comparison with pancreatic counterparts. Histopathology. 2014;65:164–173.
Adsay V, Mino-Kenudson M, Furukawa T, et al. Pathologic evaluation and reporting of intraductal papillary mucinous neoplasms of the pancreas and other tumoral intraepithelial neoplasms of pancreatobiliary tract: recommendations of Verona Consensus Meeting. Ann Surg. 2016;263:162–177.
Basturk O, Hong SM, Wood LD, et al. A revised classification system and recommendations from the baltimore consensus meeting for neoplastic precursor lesions in the pancreas. Am J Surg Pathol. 2015;39:1730–1741.
Torbenson MS. Hamartomas and malformations of the liver. Semin Diagn Pathol. 2019;36:39–47.
Mamone G, Carollo V, Cortis K, et al. Magnetic resonance imaging of fibropolycystic liver disease: the spectrum of ductal plate malformations. Abdom Radiol (NY). 2019;44:2156–2171.
Wills ES, Roepman R, Drenth JP. Polycystic liver disease: ductal plate malformation and the primary cilium. Trends Mol Med. 2014;20:261–270.
Nakanuma Y. Reply to “What are ductal plate and ductal plate malformations of human livers?” Liver Int. 2014;34:323.
Soares KC, Goldstein SD, Ghaseb MA, et al. Pediatric choledochal cysts: diagnosis and current management. Pediatr Surg Int. 2017;33:637–650.
Basturk O, Tan M, Bhanot U, et al. The oncocytic subtype is genetically distinct from other pancreatic intraductal papillary mucinous neoplasm subtypes. Mod Pathol. 2016;29:1058–1069.
Aapkes SE, Bernts LHP, Barten TRM, et al. Estrogens in polycystic liver disease: a target for future therapies? Liver Int. 2021;41:2009–2019.
Aapkes SE, Bernts LHP, van den Berg M, et al. Tamoxifen for the treatment of polycystic liver disease: a case report. Medicine (Baltimore). 2021;100:e26797–e26800.
Hernandez-Gonzalez A, Sanchez-Ovejero C, Manzano-Roman R, et al. Evaluation of the recombinant antigens B2t and 2B2t, compared with hydatid fluid, in IgG-ELISA and immunostrips for the diagnosis and follow up of CE patients. PLoS Negl Trop Dis. 2018;12:e0006741.
Zait H, Hamrioui B. Human cystic echinococcosis: serological diagnosis by indirect hemagglutination test, enzyme-linked immunosorbent assay, immunoelectrophoresis, and immunoblotting in surgically confirmed patients versus cases diagnosed by imaging techniques. Med Mal Infect. 2020;50:676–683.

Auteurs

Ayse Armutlu (A)

Department of Pathology, Koc University School of Medicine.

Brian Quigley (B)

Departments of Pathology.

Hegyong Choi (H)

Department of Pathology, Ulsan University Hospital, Ulsan.

Olca Basturk (O)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.

Gizem Akkas (G)

Departments of Pathology.

Burcin Pehlivanoglu (B)

Departments of Pathology.

Bahar Memis (B)

Departments of Pathology.

Kee-Taek Jang (KT)

Department of Pathology, Samsung Medical Center, Seoul, Republic of Korea.

Mert Erkan (M)

Mehmet Ali Aydınlar Acibadem University, Atakent Hospital, Istanbul.

Burcu Erkan (B)

Department of Radiology, Aydin University School of Medicine, Istanbul, Turkey.

Serdar Balci (S)

Departments of Pathology.

Burcu Saka (B)

Department of Pathology, Koc University School of Medicine.

Pelin Bagci (P)

Departments of Pathology.

Alton B Farris (AB)

Departments of Pathology.

David A Kooby (DA)

Surgery, Emory University, Atlanta, GA.

Diego Martin (D)

Department of Radiology, University of Arizona College of Medicine, Tucson, AZ.

Bobby Kalb (B)

Department of Radiology, University of Arizona College of Medicine, Tucson, AZ.

Shishir K Maithel (SK)

Surgery, Emory University, Atlanta, GA.

Juan Sarmiento (J)

Surgery, Emory University, Atlanta, GA.

Michelle D Reid (MD)

Departments of Pathology.

N Volkan Adsay (NV)

Department of Pathology, Koc University School of Medicine.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH