Concurrent Occurrence of Rectal Adenocarcinoma and Vulvar Keratinizing Squamous Cell Carcinoma: Case Report and Literature Review
Clinical Practice
Odeta Laukaitytė
Lithuanian University of Health Sciences image/svg+xml
Gustė Brazytė
Lithuanian University of Health Sciences image/svg+xml
Tadas Latkauskas
Hospital of Lithuanian University of Health Sciences Kaunas Clinics image/svg+xml
Saulius Paškauskas
Hospital of Lithuanian University of Health Sciences Kaunas Clinics image/svg+xml
Published 2025-07-24
https://doi.org/10.15388/LietChirur.2025.24(3).5
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Keywords

rectal carcinoma
vulvar carcinoma
vulvar cancer risk factors
rectal cancer risk factors
vulvar squamous cell carcinoma and rectal adenocarcinoma

How to Cite

1.
Laukaitytė O, Brazytė G, Latkauskas T, Paškauskas S. Concurrent Occurrence of Rectal Adenocarcinoma and Vulvar Keratinizing Squamous Cell Carcinoma: Case Report and Literature Review. LS [Internet]. 2025 Jul. 24 [cited 2025 Oct. 24];24(3):212-20. Available from: https://test.zurnalai.vu.lt/lietuvos-chirurgija/article/view/40010

Abstract

Introduction. Vulvar carcinoma is a rare malignancy, whereas rectal cancer is a more common oncological condition. However, the simultaneous occurrence of these two diseases is exceptionally rare. Case presentation. A 76-year-old woman presented with rectal bleeding and was previously diagnosed with keratinizing squamous cell carcinoma G1 of the vulva, unrelated to HPV. Imaging revealed tumor-like masses in the vulva and rectum, with pathological lymph nodes. Biopsy confirmed rectal adenocarcinoma in situ. She underwent obstructive rectal resection, colostomy formation, vulvar resection, and lymphadenectomy. Postoperative antibiotic therapy was administered and discontinued after seven days due to stable inflammatory markers. The patient was discharged in good condition, with planned rehabilitation in a sanatorium. Conclusion. Rectal adenocarcinoma and vulvar keratinizing squamous cell carcinoma concurrent occurrence is very rare. The risk factors for vulvar cancer (HPV, smoking, immunosuppression, lichen sclerosus) and rectal cancer (genetic predispositions, lifestyle factors (e.g., smoking, alcohol consumption), inflammatory bowel diseases) differ. However, genetic syndromes and certain interactions between lifestyle factors may lead to the concurrent occurrence of these two tumors. Given the complexity of managing two primary tumors, a multidisciplinary surgical approach was essential in our case. Further research is needed to explore possible biological links and optimize diagnostic and treatment strategies for such rare oncological presentations.

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