Case Report
Copyright ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Nov 6, 2023; 11(31): 7724-7731
Published online Nov 6, 2023. doi: 10.12998/wjcc.v11.i31.7724
Multiple inflammatory pseudotumor formation after craniopharyngioma resection via an extended nasal endoscopic approach: A case report
Hao Wu, Yu-Wei Ding, Zheng-Cun Yan, Min Wei, Xiao-Dong Wang, Heng-Zhu Zhang
Hao Wu, Department of Neurosurgery, The Second Affiliated Hospital of Xi’an Medical University, Xi'an 710038, Shaanxi Province, China
Hao Wu, Zheng-Cun Yan, Min Wei, Xiao-Dong Wang, Heng-Zhu Zhang, Department of Neurosurgery, Clinical Medical College, Yangzhou University, Yangzhou 225001, Jiangsu Province, China
Yu-Wei Ding, Department of Neurosurgery, The Yangzhou School of Clinical Medicine of Dalian Medical University, Yangzhou 225001, Jiangsu Province, China
Author contributions: Wu H contributed to manuscript writing and editing, and data collection; Ding YW, Yan ZC, Wei M, and Wang XD contributed to data analysis; Zhang HZ contributed to conceptualization and supervision; all authors have read and approved the final manuscript.
Informed consent statement: The patient provided informed written consent prior to study enrollment.
Conflict-of-interest statement: The authors report no conflicts of interest for this work.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Heng-Zhu Zhang, MD, PhD, Deputy Director, Senior Researcher, Department of Neurosurgery, Clinical Medical College, Yangzhou University, No. 98 Nantong Xi Road, Yangzhou 225001, Jiangsu Province, China. zhanghengzhu@sina.com
Received: September 12, 2023
Peer-review started: September 12, 2023
First decision: September 19, 2023
Revised: September 27, 2023
Accepted: October 17, 2023
Article in press: October 17, 2023
Published online: November 6, 2023
Processing time: 55 Days and 6.9 Hours
Abstract
BACKGROUND

This report describes a case of intracranial multiple inflammatory pseudotumors (IP) after endoscopic resection of a craniopharyngioma, which is relatively rarely reported in the literature, and neurosurgeons should be aware of its existence.

CASE SUMMARY

Herein, we report the case of a 56-year-old man who developed decreased visual acuity and blurred vision without obvious cause or inducement on April 27, 2020. To seek further treatment, he went to the Department of Neurosurgery, Clinical Medical College, Yangzhou University. After falling ill, there was no nausea, vomiting, limb convulsions, obvious disturbance of consciousness, speech disorders, cough, or persistent fever. The neurological examination findings were normal, and pituitary magnetic resonance imaging (MRI) revealed multiple nodules with abnormal signals in the sellar region. The diagnosis was craniopharyngioma. We performed total resection of the tumor via transnasal endoscopy, and the postoperative pathology suggested that the type of tumor was craniopharyngioma. Six months after the operation, the patient experienced sudden hearing loss in the right ear, tinnitus in both ears, and numbness on the right side of the face and head. Meanwhile, cranial MRI showed multiple IP. After steroid hormone and anti-inflammatory therapy, the above symptoms did not significantly improve. Finally, the patient's symptoms were well improved by surgery, and the postoperative pathological diagnosis was multiple IP.

CONCLUSION

Intracranial inflammatory pseudotumor is a benign disease with slow progression, but the clinical symptoms and imaging findings are not typical, there are no pathological findings, and the diagnosis is relatively difficult. Most of the cases are treated by surgical resection, and the prognosis is good after surgery.

Keywords: Multiple inflammatory pseudotumors; Craniopharyngioma; Treatment; Brain; Oncology; Case report

Core Tip: Inflammatory pseudotumor, also known as inflammatory myofibroblastoma, is a nodular lesion with fibrous connective tissue proliferation accompanied by a large number of inflammatory cells. The disease can occur in any part of the body, most often in the lungs, but also in the liver, spleen, lymph nodes, and other parts, and intracranial occurrence is relatively rare, especially after craniopharyngioma resection via an extended nasal endoscopic approach. The purpose of this case report is to remind clinicians of the existence of inflammatory pseudotumors after craniocerebral surgery.