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Fertility-preserving management of an inflammatory myofibroblastic tumor: A case report and review of the literature
Molecular diagnostics have broadened the categorization of mesenchymal tumors of the uterus. Knowledge of the increasing heterogeneity of uterine neoplasms is paramount for the gynecologist as the management and prognosis of these neoplasms differ from those of typical leiomyomas. In this case, a 26...
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Published in: | Case reports in women's health 2023-03, Vol.37, p.e00481, Article e00481 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Molecular diagnostics have broadened the categorization of mesenchymal tumors of the uterus. Knowledge of the increasing heterogeneity of uterine neoplasms is paramount for the gynecologist as the management and prognosis of these neoplasms differ from those of typical leiomyomas.
In this case, a 26-year-old nulligravid patient underwent hysteroscopic management for an enlarging submucosal neoplasm of the uterus. She was found to have an inflammatory myofibroblastic tumor (IMT) after ALK (anaplastic lymphoma kinase) immunostaining. Upon review of pathologic characteristics, she was treated expectantly with repeat hysteroscopy 12 months later. Ongoing conservative management will entail serial pelvic imaging.
IMTs should be considered in the differential diagnosis of fibroids presenting in young women. Fertility-preserving management in select patients is appropriate after patient counselling.
•Uterine inflammatory myofibroblastic tumors are neoplasms of indeterminate biological potential•IMTs can recur and metastasize after initial resection•Advances in molecular diagnostics allow for increased recognition of IMTs in young patients with apparent fibroid disease•Careful patient selection and counselling allows for fertility-preserving management of IMTs |
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ISSN: | 2214-9112 2214-9112 |
DOI: | 10.1016/j.crwh.2023.e00481 |