Evidence map›Paper›PMID 41924610›Full record

ArticleFrontiers in oncology2026

Eosinophilic cholangitis misdiagnosed as cholangiocarcinoma: a case report.

Yabo Hou, Xinxin Wang, Jianhua Chang, Xiaojun Yang

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yabo HouDepartment of Hepatobiliary Surgery, Gansu Provincial Hospital, Lanzhou, Gansu, China.
Xinxin WangDepartment of Hepatobiliary Surgery, Gansu Provincial Hospital, Lanzhou, Gansu, China.
Jianhua ChangDepartment of Hepatobiliary Surgery, Gansu Provincial Hospital, Lanzhou, Gansu, China.
Xiaojun YangDepartment of Hepatobiliary Surgery, Gansu Provincial Hospital, Lanzhou, Gansu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eosinophilic cholangitis (EC) has a low clinical incidence, and cases with definitive pathological confirmation are extremely rare. Due to the lack of specificity in clinical and radiologic features, EC is frequently misdiagnosed as cholangiocarcinoma. We report a 65-year-old man admitted with progressive jaundice and persistent dull right upper-quadrant abdominal pain for more than 1 month. Laboratory tests showed a markedly elevated peripheral blood eosinophil count, significantly elevated bilirubin levels, and elevated tumor markers. MRI revealed intra- and extrahepatic bile duct dilatation and common bile duct wall thickening. Cholangiocarcinoma was initially suspected. A radical pancreaticoduodenectomy was planned. However, intraoperative exploration showed edema and induration of the bile duct and pancreas. Therefore, the radical resection was aborted, and bile duct wall biopsy alone was performed for pathological diagnosis. Postoperative histopathology revealed dense eosinophilic infiltration in the bile duct wall (>20 eosinophils per high-power field), confirming the diagnosis of EC. After postoperative standard methylprednisolone therapy, the patient achieved complete symptom resolution. Laboratory indices returned to the normal range, and no recurrence was observed during the 3-month follow-up. This case highlights that EC should be suspected in biliary obstruction with unexplained eosinophilia, and histopathology is the key to definitive diagnosis.

Indexed as

eosinophiliaeosinophilic cholangitisobstructive jaundicepathological examinationsclerosing cholangitis

Identifiers

PMID41924610
PMCPMC13035734

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