期刊
JOURNAL OF PEDIATRIC SURGERY CASE REPORTS
卷 83, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.epsc.2022.102326
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Sacrococcygeal teratomas (SCT) are a rare entity, occurring in approximately 1 of every 35,000 to 40,000 births. Although it remains the most common extragonadal germ cell tumor, type IV SCT represents less than 10% of those. The diagnosis is challenging, as the initial presentation has been described as chronic pelvic pain, rectal mass and mild to severe urinary symptoms. Urinary obstruction is a rare initial presentation, described in the literature only three times. Here in, we present a rare case of type IV SCT with a complete urinary obstruction as an initial symptom.
Sacrococcygeal teratomas (SCT) are a rare entity, occurring in approximately 1 of every 35,000 to 40,000 births [1]. Although it remains the most common extragonadal germ cell tumor, type IV SCT represents less than 10% of those [1]. The diagnosis is challenging, as the initial presentation has been described as chronic pelvic pain, rectal mass and mild to severe urinary symptoms [2-4]. To our knowledge urinary obstruction is a rare initial presentation, described in the literature only three times [5-7]. Here in, we present a rare case of type IV SCT with a complete urinary obstruction as an initial symptom.
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