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01 April 2025 : Case report  Malaysia

A Complex Case of Testicular Choriocarcinoma in Cryptorchidism and Choriocarcinoma Syndrome: Clinical and Treatment Insights

Rare disease, Rare coexistence of disease or pathology

Nik Marina Nik Ibrahim ABCDEF 1, Salma Yasmin Mohd Yusuf ORCID logo DEF 1, Khariah Mat Nor ORCID logo CDEF 2, Pei Yeing Teoh ORCID logo CDEF 3, Anis Safura Ramli ORCID logo ABCDEF 1,4*

DOI: 10.12659/AJCR.946461

Am J Case Rep 2025; 26:e946461

Figure 1. Contrast-enhanced computed tomography (CECT) scan of the pelvis in axial (A) and coronal (B) planes. The images show a large heterogeneously-enhancing soft-tissue mass (indicated by blue arrows) located within the right inguinal region, extending into the right scrotal sac. It measured 13.3 cm (anterior-posterior)×15.9 cm (width)×17.4 cm (craniocaudal). There was no evidence of septation, calcification, or focal enhancing mural nodule within the mass, associated with surrounding skin thickening. It is consistent with a diagnosis of an undescended right testicular tumor. (C) Multiple enlarged matted lymph nodes (indicated by blue arrow) that appeared to be encasing the right common, external, and internal iliac arteries and veins (external iliac arteries indicated by red arrow, internal iliac arteries indicated by yellow arrow).

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923