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ArticleCase reports in obstetrics and gynecology2025

Recurrent Immature Teratoma Mimicking Growing Teratoma Syndrome Following Initial Resection: A Diagnostic Pitfall.

Shogo Nishino, Hidetaka Nomura, Takato Goto, Ryo Nimura, Yoichi Aoki, Sanshiro Okamoto, Makiko Omi, Yui Kojima, Akiko Tonooka, Hiroyuki Kanao

Abstract readCase Reports
In one paragraph

Article in Case reports in obstetrics and gynecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

10 authors.

Shogo NishinoDepartment of Gynecologic Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0001-9493-7176
Hidetaka NomuraDepartment of Gynecologic Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Takato GotoDepartment of Gynecologic Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Ryo NimuraDepartment of Gynecologic Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Yoichi AokiDepartment of Gynecologic Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Sanshiro OkamotoDepartment of Gynecologic Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Makiko OmiDepartment of Gynecologic Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Yui KojimaDivision of Pathology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Akiko TonookaDivision of Pathology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Hiroyuki KanaoDepartment of Gynecologic Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Growing teratoma syndrome (GTS) is a rare condition characterized by the enlargement of metastatic masses during or after chemotherapy for malignant germ cell tumors (GCTs), despite normalized tumor marker levels. It is defined by three criteria: (1) enlarging or new masses during or after chemotherapy, (2) normal tumor marker levels, and (3) histological presence of only mature teratoma elements. Differentiating GTS from recurrent immature teratoma is challenging, as both conditions may present similarly in imaging and tumor marker profiles. Case Presentation: We report the case of a 20-year-old woman diagnosed with a mixed ovarian GCT, consisting of grade 2 immature teratoma and yolk sac tumor. After undergoing right salpingo-oophorectomy and chemotherapy, she remained in remission for 4 years. Follow-up imaging revealed enlarged para-aortic lymph nodes. Due to normal tumor markers and a lack of response to chemotherapy, the condition was initially diagnosed as GTS, prompting surgical resection of the lymph nodes. Histopathological analysis, however, revealed immature neuroepithelial elements consistent with grade 3 immature teratoma, contradicting the GTS diagnosis. The final diagnosis was revised to recurrent immature teratoma. Conclusion: This case highlights the diagnostic challenges in distinguishing between GTS and recurrent immature teratoma. While normal tumor markers and tumor growth following chemotherapy may suggest GTS, histopathological confirmation is essential. Clinicians should maintain a high index of suspicion for recurrent immature teratoma in cases mimicking GTS and consider surgical resection for definitive diagnosis. Multidisciplinary evaluation remains crucial in the management of ovarian GCTs.

Indexed as

germ cell tumorsgrowing teratoma syndromehistopathologyimmature teratomaovarian cancer

Identifiers

PMID41195259
PMCPMC12585828

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