Laparoscopic resection of retroperitoneal intra-psoas muscle schwannoma: A case report and extensive literature review
Autor: | Safaa Allehiani, Mohammed N. AlAli, Hussein Al-Sakkaf, Sulaiman A. Al-Shammari, Awadh AlQahtani, Maria Arafah |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
Schwannoma Review Article 03 medical and health sciences Psoas muscle 0302 clinical medicine Laparoscopic anterior approach otorhinolaryngologic diseases Medicine Laparoscopic resection Laparoscopy neoplasms Neurilemoma medicine.diagnostic_test business.industry Cranial nerves Soft tissue Emergency department medicine.disease nervous system diseases 030220 oncology & carcinogenesis 030211 gastroenterology & hepatology Surgery Radiology Presentation (obstetrics) business Neurilemmoma |
Zdroj: | International Journal of Surgery Case Reports |
ISSN: | 2210-2612 |
Popis: | Highlights • Retroperitoneal schwannoma is a rare disease and needs a high index of suspicion to be diagnosed. • Generally, retroperitoneal schwannomas are known to be non-sensitive either to radiation or to chemotherapy. • Retroperitoneal schwannomas therefore, requiring complete surgical excision with negative margins. • In retroperitoneal schwannomas, due to the presence of multiple surgical approaches and different presentations, surgical access should be individualized. Introduction Soft tissue tumors of Schwann cells in either the peripheral or cranial nerves are known as schwannomas or also as neurilemmomas. Limited data exists regarding psoas muscle schwannoma in the literature. Therefore, we have done an extensive literature review and found a total number of 46 cases of intra-psoas schwannoma including our case, which are summarized in this article along with reporting our new case. Presentation of case We report a very rare case of primary left intra-psoas muscle schwannoma in a 39-year-old Saudi gentleman, smoker with an unremarkable medical and surgical history. The patient presented to the emergency department with exacerbated chronic lower abdominal pain since almost 2 years. After conforming the diagnosis, the patient was admitted electively and underwent uneventful laparoscopic hand-assisted resection. Discussion Schwannomas are neurogenic tumors which known to be solitary, benign, well circumscribed, encapsulated, and slow-growing tumors. Multiple imaging modalities are used to detect such a tumor. Although there is no consensus on the best surgical approach, endoscopic mini-laparotomy, laparoscopy (anterior [as in our case] or lateral), and robotic resection were reported with good outcomes. Conclusion Retroperitoneal schwannoma and intra-psoas muscle variant are a rare entity, with slow growing rate and risk of malignant transformation. Therefore, high index of suspicion, good follow-up, and large-cohort studies are encouraged. |
Databáze: | OpenAIRE |
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