Retroperitoneal schwannoma: An abnormal presentation mimicking a pelvic mass

Introduction: A schwannoma is an encapsulated nerve sheath tumor originating from differentiated Schwann cells. Schwannomas are preferentially localized to the head, neck, and extremities with a minor occurrence of 1–3% in the retroperitoneal space. Schwannomas are often asymptomatic due to slow growth but can be present with symptoms according to their location. We report a case of a 45-year-old female with a retroperitoneal schwannoma that initially was suspected to be an ovarian mass. Case Report: A 45-year-old female with a 10-year history of a right ovarian cyst presented with lower abdominal pain, early satiety, hematuria, low back pain and constipation. Transabdominal ultrasound showed right ovarian enlargement measuring 8.8 × 6.6 cm, described as heterogeneous with loculations. Tumor markers indicated a low risk of malignancy. The patient was taken to the operating room for an exploratory laparotomy that revealed a large, firm posterior pelvic mass palpated in the retroperitoneal space. The cyst wall could not be completely dissected due to proximity to major vessels and nerve roots. The patient was referred to a neighboring academic institution because of the case complexity. She underwent repeat exploratory laparotomy and neuroplasty of the L5, S1, and S2 nerve roots. The L5 nerve root was ultimately sacrificed and the retroperitoneal mass was removed. Final pathology revealed a benign schwannoma. Conclusion: The diagnosis of a retroperitoneal schwannoma is often missed because of its rare occurrence, location, vague symptoms, and resemblance to other tumors on varying imaging modalities. Due to low incidence and often delay in diagnosis, current management guidelines are limited. Currently, histopathological exam after total surgical resection is the most reliable source for diagnosis. The patient in this case demonstrates the need for improvement in the preoperative evaluation and consideration of non-gynecologic differential diagnoses in the evaluation of a suspected pelvic mass.

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Journal
Journal of Case Reports and Images in Obstetrics and Gynecology
Published
2025-08-27
DOI
https://doi.org/10.5348/100212z08is2025cr
Primary Topic
Neurofibromatosis and Schwannoma Cases
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article
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article

Retroperitoneal schwannoma: An abnormal presentation mimicking a pelvic mass

Cameron Stokes, S. A. Seligman, Corey Reeves, Isabella Sciacca
Journal of Case Reports and Images in Obstetrics and Gynecology
Neurofibromatosis and Schwannoma Cases
article

Retroperitoneal schwannoma: An abnormal presentation mimicking a pelvic mass

Cameron Stokes, S. A. Seligman, Corey Reeves, Isabella Sciacca
article en

Abstract

Introduction: A schwannoma is an encapsulated nerve sheath tumor originating from differentiated Schwann cells. Schwannomas are preferentially localized to the head, neck, and extremities with a minor occurrence of 1–3% in the retroperitoneal space. Schwannomas are often asymptomatic due to slow growth but can be present with symptoms according to their location. We report a case of a 45-year-old female with a retroperitoneal schwannoma that initially was suspected to be an ovarian mass. Case Report: A 45-year-old female with a 10-year history of a right ovarian cyst presented with lower abdominal pain, early satiety, hematuria, low back pain and constipation. Transabdominal ultrasound showed right ovarian enlargement measuring 8.8 × 6.6 cm, described as heterogeneous with loculations. Tumor markers indicated a low risk of malignancy. The patient was taken to the operating room for an exploratory laparotomy that revealed a large, firm posterior pelvic mass palpated in the retroperitoneal space. The cyst wall could not be completely dissected due to proximity to major vessels and nerve roots. The patient was referred to a neighboring academic institution because of the case complexity. She underwent repeat exploratory laparotomy and neuroplasty of the L5, S1, and S2 nerve roots. The L5 nerve root was ultimately sacrificed and the retroperitoneal mass was removed. Final pathology revealed a benign schwannoma. Conclusion: The diagnosis of a retroperitoneal schwannoma is often missed because of its rare occurrence, location, vague symptoms, and resemblance to other tumors on varying imaging modalities. Due to low incidence and often delay in diagnosis, current management guidelines are limited. Currently, histopathological exam after total surgical resection is the most reliable source for diagnosis. The patient in this case demonstrates the need for improvement in the preoperative evaluation and consideration of non-gynecologic differential diagnoses in the evaluation of a suspected pelvic mass.

Journal of Case Reports and Images in Obstetrics and GynecologyVol. 11(2)
University of North Texas (US), University of North Texas Health Science Center (US), The University of Texas at Arlington (US)
Openalex Percentile: Top 67%
Neurofibromatosis and Schwannoma Cases
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