Adult sacrococcygeal teratoma

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We report a case of adenocarcinoma arising from a sacrococcygeal mature teratoma in an adult female. A year-old female was diagnosed with a presacral tumor 10 years ago. Pelvic computed tomography CT demonstrated a presacral heterogeneous tumor, containing multiloculated cystic area and enhanced solid component with calcification.

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A sacrococcygeal teratoma SCT is a congenital present at birth growth or tumour that develops at the base of the spine just above the buttocks. It is the most common neonatal newborn tumour, affecting about 1 in every 40, babies born. A SCT can grow to quite a large size while the baby is in the womb, sometimes a similar size to the baby.

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Click on image for details. Correspondence Address : Dr. The aim of the present study was to know the frequency of teratomas in various sites and to analyze their clinicomorphological features.

The Internet Journal of Surgery. Background: Sacrococcygeal teratomas [SCT] are derived from embryonic germ-cell layers and are mostly encountered in infants. In adults, this entity is extremely rare and always worrisome for malignancy.

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Sacrococcygeal teratomas are congenital neoplasms with a prevalence of 1 in 40, live births. Microscopically, teratomas are often disorganized and contain differentiated tissues from all three germ cell layers. Although these lesions are usually benign, the risk of malignant transformation increases significantly with advancing age. When teratomas recur, they tend to do so within 2 years of resection.

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Correspondence Address : Dr. Sacrococcygeal tumors are present most frequently in infancy and childhood. Incidence in the newborn is 1 in with a female to male ratio of

To determine the clinical, imaging, and histological features, and surgical resection modalities and outcomes of adult sacrococcygeal teratoma SCT. Adult patients with histopathologically diagnosed SCT were enrolled in our hospital between August and August There were 8 patients in the study 2 males, 6 females with a median age of 34 years range, 18—67 years. The time to clinical symptoms was 14 d to 35 years, with a median time of 4 years.

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