Malignant Ovarian Steroid Cell Tumor, Not Otherwise Specified, Causes Virilization in a 4-Year-Old Girl: A Case Report and Literature Review.

Chemotherapy Child Not otherwise specified Ovary Steroid cell tumor

Journal

Case reports in oncology
ISSN: 1662-6575
Titre abrégé: Case Rep Oncol
Pays: Switzerland
ID NLM: 101517601

Informations de publication

Date de publication:
Historique:
received: 16 01 2020
accepted: 16 01 2020
entrez: 2 5 2020
pubmed: 2 5 2020
medline: 2 5 2020
Statut: epublish

Résumé

We report a case of a 4-year-old girl with an ovarian steroid cell tumor, not otherwise specified (SCT-NOS). She was admitted to the hospital with progressing virilization and Cushing's syndrome, which included abnormality of the perineum, hirsutism, hypertrichosis, flushing of face, hoarseness, and weight gain. Blood testing showed a significantly increased testosterone level and slightly increased cortisol level. Computed tomography scan revealed an 8.0 × 5.0 × 5.0 cm tumor of the right ovary. The patient underwent right salpingo-oophorectomy, and pathological examination showed malignant potential. Three courses of bleomycin, etoposide, and cisplatin were administered as postoperative chemotherapy. After tumor resection, her testosterone decreased to undetectable levels. However, during the course of the treatment, the patient suffered from adrenal insufficiency resulting in the need for hydrocortisone replacement therapy. Although SCT-NOS in childhood are typically benign, pathological findings should be carefully observed for potential malignancy. In cases of cortisol-producing SCT-NOS, serum levels should be monitored, and hydrocortisone replacement therapy should be considered before resection.

Identifiants

pubmed: 32355490
doi: 10.1159/000506044
pii: cro-0013-0358
pmc: PMC7184839
doi:

Types de publication

Case Reports

Langues

eng

Pagination

358-364

Informations de copyright

Copyright © 2020 by S. Karger AG, Basel.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to declare.

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Auteurs

Takaharu Yoshimatsu (T)

Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.

Kozo Nagai (K)

Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.

Reiji Miyawaki (R)

Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.

Kyoko Moritani (K)

Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.

Kazuhiro Ohkubo (K)

Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.
Department of Community and Emergency Medicine, Ehime University Graduate School of Medicine, Toon, Japan.

Jun Kuwabara (J)

Department of Pediatric Surgery, Ehime University Graduate School of Medicine, Toon, Japan.

Kyosuke Tatsuta (K)

Department of Pediatric Surgery, Ehime University Graduate School of Medicine, Toon, Japan.

Mie Kurata (M)

Department of Analytical Pathology, Ehime University Graduate School of Medicine, Toon, Japan.
Proteoscience Center Division of Pathology, Ehime University Graduate School of Medicine, Toon, Japan.

Mana Fukushima (M)

Division of Diagnostic Pathology, Ehime University Hospital, Toon, Japan.

Riko Kitazawa (R)

Division of Diagnostic Pathology, Ehime University Hospital, Toon, Japan.

Junpei Hamada (J)

Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.

Fumihiro Ochi (F)

Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.

Minenori Eguchi-Ishimae (M)

Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.

Hisamichi Tauchi (H)

Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.

Mariko Eguchi (M)

Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.

Classifications MeSH