A Potential Case of Tubulocystic Ductal Carcinoma of the Pancreas

We present a case of pancreatic ductal carcinoma with a microcystic appearance. A 64-year-old woman was found to have a pancreatic mass during a routine medical checkup. The tumor was well-circumscribed and multicystic; thus, she was followed up for suspected serous cystadenoma. However, the tumor gradually enlarged in the following 2.5 years; subsequently, she underwent a Whipple procedure. Grossly, the cut surface of the tumor was honeycomb-like with small cysts. Histologically, the cysts were ductal structures lined by a relatively bland, cuboidal or columnar epithelium with mildly enlarged nuclei. No intracytoplasmic mucus was observed. The presence of stromal invasion confirmed the diagnosis of ductal carcinoma. KRAS was wild type. Postoperative course was uneventful, with no recurrence to date (followup period: 5.5 years postsurgery). The present case did not meet any known subtypes of pancreatic ductal carcinoma. The tumor resembled a large duct variant, which typically shows a microcystic appearance. However, unlike the present case, the large duct type usually consists of mucus-rich neoplastic cells. A recent study on cholangiocarcinoma proposed a novel tubulocystic subtype characterized by microcystic neoplastic glands and adenofibromatous stroma, which is morphologically similar to the present case. The present case may correspond to a pancreatic counterpart of tubulocystic cholangiocarcinoma.

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Journal
Pathology International
Published
2025-04-17
DOI
https://doi.org/10.1111/pin.70008
Citations
1
Primary Topic
Pancreatic and Hepatic Oncology Research
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article
Field-Weighted Citation Impact
1.05
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article

A Potential Case of Tubulocystic Ductal Carcinoma of the Pancreas

Tomonori Tanaka, Rena Uno, Keitaro Sofue, Yoh Zen et al.
1 citations
Pathology International
Pancreatic and Hepatic Oncology Research
1.05
article

A Potential Case of Tubulocystic Ductal Carcinoma of the Pancreas

Tomonori Tanaka, Rena Uno, Keitaro Sofue, Yoh Zen, Hirochika Toyama, Tomoo Itoh, Takumi Fukumoto
article en
1 citations

Abstract

We present a case of pancreatic ductal carcinoma with a microcystic appearance. A 64-year-old woman was found to have a pancreatic mass during a routine medical checkup. The tumor was well-circumscribed and multicystic; thus, she was followed up for suspected serous cystadenoma. However, the tumor gradually enlarged in the following 2.5 years; subsequently, she underwent a Whipple procedure. Grossly, the cut surface of the tumor was honeycomb-like with small cysts. Histologically, the cysts were ductal structures lined by a relatively bland, cuboidal or columnar epithelium with mildly enlarged nuclei. No intracytoplasmic mucus was observed. The presence of stromal invasion confirmed the diagnosis of ductal carcinoma. KRAS was wild type. Postoperative course was uneventful, with no recurrence to date (followup period: 5.5 years postsurgery). The present case did not meet any known subtypes of pancreatic ductal carcinoma. The tumor resembled a large duct variant, which typically shows a microcystic appearance. However, unlike the present case, the large duct type usually consists of mucus-rich neoplastic cells. A recent study on cholangiocarcinoma proposed a novel tubulocystic subtype characterized by microcystic neoplastic glands and adenofibromatous stroma, which is morphologically similar to the present case. The present case may correspond to a pancreatic counterpart of tubulocystic cholangiocarcinoma.

Pathology InternationalVol. 75(5)
Kobe University Hospital (JP), King's College Hospital (GB), Hyogo Prefectural Cancer Center (JP), Kobe University (JP)
Good health and well-being
Openalex Percentile: Top 23%
Pancreatic and Hepatic Oncology Research
1.05
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