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Autoimmune alopecia areata due to thymoma without myasthenia gravis: a case report

Authors :
Yukino Saito
Tomohiro Yazawa
Toshiteru Nagashima
Yoichi Ohtaki
Natsuko Kawatani
Eiji Narusawa
Ryohei Yoshikawa
Nozomi Matsumura
Tatsuro Maehara
Ken Shirabe
Source :
Surgical Case Reports, Vol 9, Iss 1, Pp 1-4 (2023)
Publication Year :
2023
Publisher :
SpringerOpen, 2023.

Abstract

Abstract Background Thymoma is associated with autoimmune diseases. Myasthenia gravis is frequently associated with thymoma, but cases of thymoma complicated by alopecia areata are very rare. In this report, we present a case of thymoma associated with alopecia areata, but without Myasthenia gravis. Case presentation A 60-year-old woman had a complaint of rapid progression of alopecia areata. A hair follicular biopsy was performed, which showed the infiltration of CD8-positive lymphocytes. She was prescribed topical steroids for 2 months prior to surgery, but her hair loss was not improved. Screening computed tomography showed a mass in the anterior mediastinum, which was suspected to be a thymoma. Myasthenia gravis was ruled out because she had no relevant symptoms or physical findings, and no anti-acetylcholine receptor antibodies were detected in serum. We performed a transsternal extended thymectomy based on a diagnosis of thymoma Masaoka stage I, without myasthenia gravis. Pathological examination showed Type AB thymoma, Masaoka stage II. The chest drainage tube was removed on postoperative day 1, and the patient was discharged on postoperative day 6. The patient has continued topical steroids and showed improvement 2 months postoperatively. Conclusions Although alopecia areata is a rare complication in thymoma cases without myasthenia gravis, thoracic surgeons need to keep this condition in mind because alopecia reduces the patient's quality of life.

Details

Language :
English
ISSN :
21987793
Volume :
9
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Surgical Case Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.469c8095234a0691e06e66229fb663
Document Type :
article
Full Text :
https://doi.org/10.1186/s40792-023-01655-2