Diagnostic and therapeutic strategies in pancreatic adenosquamous carcinoma: Molecular and clinical insights in managing metastatic disease

Nathaniel Grabill, MD; Mena Louis, DO; Mariah Cawthon, MD; Claudia Gherasim, MD; James Chambers, MD

Radiology Case Reports (Dec 2024)

Diagnostic and therapeutic strategies in pancreatic adenosquamous carcinoma: Molecular and clinical insights in managing metastatic disease

Nathaniel Grabill, MD,
Mena Louis, DO,
Mariah Cawthon, MD,
Claudia Gherasim, MD,
James Chambers, MD

Affiliations

Nathaniel Grabill, MD: Northeast Georgia Medical Center, General Surgery Department, Gainesville, GA 30501, USA; Corresponding author.
Mena Louis, DO: Northeast Georgia Medical Center, General Surgery Department, Gainesville, GA 30501, USA
Mariah Cawthon, MD: Northeast Georgia Medical Center, General Surgery Department, Gainesville, GA 30501, USA
Claudia Gherasim, MD: Northeast Georgia Medical Center, Pathology Department, Gainesville, GA 30501, USA
James Chambers, MD: Northeast Georgia Medical Center, General Surgery Department, Braselton, GA 30517, USA

Journal volume & issue: Vol. 19, no. 12
pp. 6016 – 6026

Abstract

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Adenosquamous carcinoma of the pancreas (ASCP) is a rare and aggressive variant of pancreatic cancer, characterized by both adenocarcinoma and squamous cell carcinoma components. It presents significant diagnostic and therapeutic challenges due to its atypical histology and poor prognosis. A 72-year-old male presented with abdominal pain, lighter-colored stools, and intermittent nausea. Initial imaging revealed a complex mass in the distal pancreatic body and tail. Elevated lipase levels and subsequent endoscopic ultrasound-guided fine-needle biopsy (EUS-FNB) suggested an atypical pancreatic lesion with keratinizing squamous cells.Further investigation through fiberoptic bronchoscopy and EBUS-guided transbronchial needle aspiration (TBNA) confirmed carcinoma with squamous differentiation. Genetic testing identified KRAS G12D and PIK3CA mutations. The multidisciplinary tumor board recommended systemic chemotherapy with mFOLFIRINOX and G-CSF support. The patient underwent twelve cycles of mFOLFIRINOX with dose adjustments for thrombocytopenia and effective management of chemotherapy-related side effects. Restaging CT scans showed a decrease in tumor size and stable metastatic nodes. The patient showed a partial biochemical response with decreasing CA 19-9 levels and disease stabilization on imaging. This case demonstrates the critical role of a multidisciplinary approach in managing rare pancreatic malignancies. ASCP requires a comprehensive diagnostic and therapeutic strategy involving advanced imaging, histopathological confirmation, and personalized chemotherapy. Integrating advanced diagnostic techniques, molecular profiling, and a multidisciplinary approach is essential for improving patient outcomes and providing comprehensive care for this challenging malignancy. Addressing the psychological aspects and offering compassionate care are vital for supporting patients through their treatment journey.

Published in Radiology Case Reports

ISSN: 1930-0433 (Online)
Publisher: Elsevier
Country of publisher: United States
LCC subjects: Medicine: Medicine (General): Medical physics. Medical radiology. Nuclear medicine
Website: https://www.sciencedirect.com/journal/radiology-case-reports

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Abstract

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