The Mystery of Elevated β-hCG in GnRH-Independent Precocious Puberty without a Detectable Tumor: A Six-Year Diagnostic Odyssey
HORMONE RESEARCH IN PAEDIATRICS, 2025 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Basım Tarihi: 2025
- Doi Numarası: 10.1159/000549889
- Dergi Adı: HORMONE RESEARCH IN PAEDIATRICS
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, Chemical Abstracts Core, EMBASE, MEDLINE
- Ankara Üniversitesi Adresli: Hayır
Özet
Introduction: beta-human chorionic gonadotrophin (beta-hCG) secreting tumors causing gonadotropin-independent precocious puberty (GIPP) are rare. This case underscores the diagnostic difficulties presented by these tumors. Case Presentation: A 10.8-year-old boy was referred with rapidly advancing puberty. He had Tanner stage 5 pubic hair, macropenis, accelerated growth and bone age. Suppressed gonadotropins with elevated testosterone and beta-hCG levels led to diagnosis of GIPP. Cranial imaging for the source of beta-hCG identified a 7-mm pituitary adenoma; however, resection of the pituitary lesion and petrosal sinus and cerebrospinal fluid beta-hCG measurements did not support this. A testicular biopsy and spermatic venous beta-hCG levels due to testicular calcifications indicated no evidence of testicular secretion. PET/CT demonstrated mild fluorodeoxyglucose uptake in the thymic region. Excisional biopsy was consistent with thymic hyperplasia. During follow-up, beta-hCG levels fluctuated between 100 and 154 mIU/mL, with serial imaging (cranial, thoraco-abdomino-pelvic magnetic resonance imaging) remaining unremarkable. At sixth year of follow-up, beta-hCG surged to 2,039 mIU/mL, at which time, thoracic CT revealed a 5 cm mass in the mediastinum. The mass was resected and pathology was consistent a mixed germ cell tumor. Conclusion: The source of beta-hCG may remain obscure for a long time in beta-hCG-mediated GIPP. Ongoing surveillance is essential in similar cases.