{"title":"产前发现的肾上腺未成熟畸胎瘤：病例报告和文献综述","authors":"Nishkala Rao , Amrit Kaur , Arunkumar A.R. , Prakruthi S.K. , Vinay Jadhav , Suma M.N.","doi":"10.1016/j.phoj.2024.08.004","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Teratomas are germ cell tumors derived from totipotent cells, with presentation outside the gonads being rare, and adrenal location being even rarer. Prenatally detected adrenal teratomas are extremely uncommon.</p></div><div><h3>Case report</h3><p>We report a rare case of a 5-month-old girl with a prenatally detected left suprarenal mass, which was initially suspected to be a congenital neuroblastoma. Abdominal computed tomography showed a cystic lesion measuring 7.9 x 8.8 × 11.5 cm in the left suprarenal region compatible with adrenal teratoma. The infant underwent laparotomy with excision of the lesion. The histopathological diagnosis was cystic immature teratoma.</p></div><div><h3>Conclusion</h3><p>Although adrenal teratoma is extremely rare, it should be included in the clinical and radiologic differential diagnosis of prenatally detected suprarenal masses.</p></div>","PeriodicalId":101004,"journal":{"name":"Pediatric Hematology Oncology Journal","volume":"9 4","pages":"Pages 279-282"},"PeriodicalIF":0.0000,"publicationDate":"2024-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2468124524000731/pdfft?md5=53b01dc0d97f8eb4bed00a71446339d3&pid=1-s2.0-S2468124524000731-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Prenatally detected adrenal immature teratoma: A case report and review of literature\",\"authors\":\"Nishkala Rao , Amrit Kaur , Arunkumar A.R. , Prakruthi S.K. , Vinay Jadhav , Suma M.N.\",\"doi\":\"10.1016/j.phoj.2024.08.004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Teratomas are germ cell tumors derived from totipotent cells, with presentation outside the gonads being rare, and adrenal location being even rarer. Prenatally detected adrenal teratomas are extremely uncommon.</p></div><div><h3>Case report</h3><p>We report a rare case of a 5-month-old girl with a prenatally detected left suprarenal mass, which was initially suspected to be a congenital neuroblastoma. Abdominal computed tomography showed a cystic lesion measuring 7.9 x 8.8 × 11.5 cm in the left suprarenal region compatible with adrenal teratoma. The infant underwent laparotomy with excision of the lesion. The histopathological diagnosis was cystic immature teratoma.</p></div><div><h3>Conclusion</h3><p>Although adrenal teratoma is extremely rare, it should be included in the clinical and radiologic differential diagnosis of prenatally detected suprarenal masses.</p></div>\",\"PeriodicalId\":101004,\"journal\":{\"name\":\"Pediatric Hematology Oncology Journal\",\"volume\":\"9 4\",\"pages\":\"Pages 279-282\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-08-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2468124524000731/pdfft?md5=53b01dc0d97f8eb4bed00a71446339d3&pid=1-s2.0-S2468124524000731-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pediatric Hematology Oncology Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468124524000731\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Hematology Oncology Journal","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468124524000731","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景畸胎瘤是由全能细胞衍生的生殖细胞肿瘤，在性腺以外的部位出现非常罕见，而位于肾上腺的畸胎瘤则更为罕见。病例报告 我们报告了一例罕见病例，一名 5 个月大的女孩在产前发现左肾上腺上肿块，起初怀疑是先天性神经母细胞瘤。腹部计算机断层扫描显示，左肾上区有一个 7.9 x 8.8 × 11.5 厘米的囊性病变，与肾上腺畸胎瘤相符。婴儿接受了开腹手术，切除了病灶。结论虽然肾上腺畸胎瘤极为罕见，但应将其纳入产前发现的肾上腺上肿块的临床和放射学鉴别诊断中。
Prenatally detected adrenal immature teratoma: A case report and review of literature
Background
Teratomas are germ cell tumors derived from totipotent cells, with presentation outside the gonads being rare, and adrenal location being even rarer. Prenatally detected adrenal teratomas are extremely uncommon.
Case report
We report a rare case of a 5-month-old girl with a prenatally detected left suprarenal mass, which was initially suspected to be a congenital neuroblastoma. Abdominal computed tomography showed a cystic lesion measuring 7.9 x 8.8 × 11.5 cm in the left suprarenal region compatible with adrenal teratoma. The infant underwent laparotomy with excision of the lesion. The histopathological diagnosis was cystic immature teratoma.
Conclusion
Although adrenal teratoma is extremely rare, it should be included in the clinical and radiologic differential diagnosis of prenatally detected suprarenal masses.
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