학술논문

A Case of Testicular Teratoma That Was Initially Suspected to Be a Testicular Cyst / 出生前診断された陰囊内精巣腫瘍の1例
Document Type
Journal Article
Source
日本小児外科学会雑誌 / Journal of the Japanese Society of Pediatric Surgeons. 2019, 55(7):1187
Subject
neonate
prenatal diagnosis
testicular simple cyst
testicular teratoma
testicular tumor
出生前診断
新生児
精巣囊胞
精巣奇形腫
精巣腫瘍
Language
Japanese
ISSN
0288-609X
2187-4247
Abstract
The patient in the present case was a 2-day-old boy with a cystic lesion in his left testis, which was detected during the prenatal period by a maternal ultrasound examination at 34 weeks of gestation. At 37 weeks of gestational age, the 2,890 g boy was delivered by caesarean section. A cystic lesion of 10 mm size was recognized in a postnatal imaging examination, but no apparent solid or fat component was noted. A simple cyst or an epidermoid cyst was suspected. Considering the possibility of testicular atrophy due to a cystic lesion, we performed an operation at 1 month of age, which revealed a monoclastic cyst with a clear edge, which only nucleated the cyst. Histopathological analysis revealed squamous epithelial cells on the cyst wall surface, fibromuscular tissue, and intestinal tissue. Mature cystic teratoma was the diagnosis based on the examination findings of extirpated tissue. As shown in this case, the prenatal diagnosis of testicular tumors in the scrotum is very rare. In this case, a simple testicular cyst was initially considered to be the most likely diagnosis because no solid component was recognized on imaging after birth. In neonatal patients with testicular tumors, even lesions that only contain a cyst require a careful diagnosis and treatment with the possibility of germ cell tumors kept in mind.