[A Case of Acinar Cell Carcinoma-Difficult to Differentiate on Imaging Pre-Laparoscopic Distal Pancreatectomy]

Mao Nakade1, Shinsuke Nakashima, Hirotoshi Takayama

  • 1Dept. of Gastroenterological Surgery, Higashiosaka City Medical Center.

Insights

A rare case of acinar cell carcinoma (ACC) presented as a cystic pancreatic mass. Surgical resection led to a 5-year recurrence-free survival, highlighting ACC in pancreatic mass differential diagnosis.

Area of Science:

  • Oncology
  • Gastroenterology
  • Radiology

Background:

  • Pancreatic cystic neoplasms present a diagnostic challenge.
  • Acinar cell carcinoma (ACC) is a rare pancreatic malignancy.
  • Distinguishing ACC from other cystic lesions is crucial for appropriate management.

Purpose of the Study:

  • To report a case of acinar cell carcinoma (ACC) initially suspected as a mucinous cystic neoplasm (MCN).
  • To illustrate the imaging characteristics of ACC on CT and MRI.
  • To emphasize the importance of considering ACC in the differential diagnosis of mixed cystic and enhancing pancreatic masses.

Main Methods:

  • Contrast-enhanced CT and MRI were utilized for initial characterization of the pancreatic mass.
  • Laparoscopic distal pancreatectomy was performed for suspected MCN.
  • Immunohistochemical staining (BCL-10 and trypsin) was used for definitive diagnosis.

Main Results:

  • A 33 mm pancreatic cystic mass with an enhancing component was identified.
  • Imaging revealed specific signal characteristics on diffusion-weighted images and ADC maps.
  • Immunostaining confirmed the diagnosis of acinar cell carcinoma (ACC).
  • The patient remained recurrence-free for 5 years post-surgery without further treatment.

Conclusions:

  • Acinar cell carcinoma (ACC) can present as a cystic pancreatic mass with enhancing components.
  • Multimodality imaging is essential for characterizing pancreatic lesions.
  • ACC should be included in the differential diagnosis for mixed cystic and enhancing pancreatic masses.

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