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Relevant bibliographies by topics / Sacrococcygeal teratoma(SCT)

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Academic literature on the topic 'Sacrococcygeal teratoma(SCT)'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Sacrococcygeal teratoma(SCT)"

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Daksha, Shraddha, Shakti Bhan Khanna, Kiranabala Dash, Shuaib Zaidi, and Vikas Kashyap. "Asymptomatic adult type IV sacrococcygeal teratoma: incidental diagnosis in a case of subfertility." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 13, no. 11 (2024): 3405–8. http://dx.doi.org/10.18203/2320-1770.ijrcog20243219.

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Sacrococcygeal teratomas (SCT) are rare congenital tumours that are even more uncommon when present in adulthood. They are derived from residual stem cells in the presacral space that differentiate into clusters of somatic cells. We present a case of asymptomatic sacrococcygeal teratoma (SCT) in 28 years old female, presented for subfertility workup and diagnosed incidentally while investigating for it. Preoperative diagnosis was complex cystic lesion involving presacral space with possibility of dermoid, epidermal, or cystic presacral hamartoma. The mass was completely excised through abdomen

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Nasreen, Ali* &. Sunil Kumar Agarwalla. "MALIGNANT SACROCOCCYGEAL TERATOMA IN AN INFANT-RARE CASE REPORT." Indian Journal of Medical Research and Pharmaceutical Sciences 4, no. 6 (2017): 28–30. https://doi.org/10.5281/zenodo.810281.

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Sacrococcygeal teratoma(SCT) is a tumour located at the base of coccyx (tail bone) and thought to be derived from embryonic germ cell layers.The tumors present mostly in infancy. Modern imaging techniques may be helpful to detect the extent of mass. Here we report a case of 1 year old female baby who presented to the emergency department of MKCG with complains of anuria and constipation for last 4 days.The abdomen was distended.USG abdomen and pelvis and CECT abdomen showed mass in the sacro coccygeal area.FNAC confirmed the diagnosis as MALIGNANT GERM CELL SACROCOCCYGEAL TERATOMA. Most sacroc

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Vaitkevičiūtė, Marija, Saulė Kržčonavičiūtė, Eglė Savukynė, Eglė Machtejevienė, and Ieva Rubavičiūtė. "Antenatalinė kryžkaulio-uodegikaulio cistinės teratomos diagnostika. Klinikinis atvejis ir literatūros apžvalga." Lithuanian Obstetrics & Gynecology 25, no. 3 (2022): 240–45. http://dx.doi.org/10.37499/lag.993.

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Kryžkaulio-uodegikaulio teratoma (angl. sacrococcygeal teratoma – SCT) yra įgimtas embrioninis navikas, dažniau diagnozuojamas moteriškosios lyties vaisiams ir naujagimiams. Šiame straipsnyje aprašomas retas antenatalinis vaisiaus kryžkaulio-uodegikaulio cistinės teratomos klinikinis atvejis, nustatytas 2022 m., Lietuvos sveikatos mokslų universiteto ligoninės Kauno klinikų (toliau – Kauno klinikų) Akušerijos ir ginekologijos klinikoje. Literatūros apžvalgoje aprašoma kryžkaulio-uodegikaulio cistinės teratomos diferencinė diagnozė. Ypatingas dėmesys skiriamas terminalinės mielocistocelės ir SC

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Sabir, Wirya N., Sasan M. Ahmed, Karzan M. Hasan, et al. "Giant sacrococcygeal teratoma in an infant: a case report with a literature review." Annals of Medicine & Surgery 85, no. 11 (2023): 5666–69. http://dx.doi.org/10.1097/ms9.0000000000001274.

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Introduction and importance: A sacrococcygeal teratoma (SCT) is a rare embryonal tumor that emerges in the sacrococcygeal area. It affects one in every 35 000–40 000 live births. Herein, we report a case of a substantial SCT in a neonate. Case presentation: A neonate girl from consanguineous parents was delivered by cesarean section with a large mass (18×17 cm) in the sacrococcygeal area. The baby’s birth weight was 5 kg, of which 2.5 belonged to the mass. The vital signs were within normal ranges and she had weak movement with bluish peripheral limbs. Oxygen saturation was around 85% for a sh

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5

Shahjouei, Shima, Sara Hanaei, Farideh Nejat, Maryam Monajemzadeh, and Mostafa El Khashab. "Sacrococcygeal teratoma with intradural extension: case report." Journal of Neurosurgery: Pediatrics 15, no. 4 (2015): 380–83. http://dx.doi.org/10.3171/2014.10.peds1445.

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Intradural sacrococcygeal teratoma (SCT) is a rare entity that has been reported in only a few cases previously. The authors present the case of a 2-week-old, otherwise healthy neonate with a mass in the buttock. The imaging findings and the high level of serum alpha-fetoprotein were highly suggestive of SCT. On operation the authors found intradural extension of the teratoma. The lesion was managed successfully without any remaining sequelae. The authors briefly review the currently proposed etiology regarding teratoma formation and the intradural extension of SCT.

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Kundal, VK, A. Jadhav, A. Gupta, A. Shukla, V. Chaturvedi, and R. Kundal. "Sacrococcygeal Teratoma: Experience with 36 Patients in a Teritiary Care Hospital." Journal of Nepal Paediatric Society 35, no. 1 (2015): 89–93. http://dx.doi.org/10.3126/jnps.v35i1.10945.

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Introduction: Sacrococcygeal teratomas (SCT) are the most common solid tumours in the neonatal period, originate from embryonic totipotent cells. Most of them are benign however some that present later in life and have major intra-pelvic component have greater malignant potential. Complete surgical excision provides an excellent prognosis. The aim of this study was to describe the clinical profile, age of presentation, sex distribution, diagnostic evaluation and management of children with a histological confirmed diagnosis of sacrococcygeal teratoma.Material and Methods: Patients with histolo

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7

M, Parvez, Paul S. K, Muaz S. S. A, Rahman A, Hasan S, and Alam J. "Childhood Sacrococcygeal Teratoma: A Histopathological Study." Saudi Journal of Medical and Pharmaceutical Sciences 8, no. 12 (2022): 809–12. http://dx.doi.org/10.36348/sjmps.2022.v08i12.014.

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Background: Sacrococcygeal teratoma (SCT) is a relatively uncommon germ cell tumor and affecting neonates, infants as well as children with a female preponderance. Age is an important predictor of malignancy in SCT. Early diagnosis and management can provide better outcome. Histologically most of the cases are benign in nature. Aim: Since there have been paucity of sufficient studies in this field in Bangladesh. The present study was carried out to describe in various clinicopathological features and histopathological findings of SCT patients. Materials and Methods: The study included 66 patie

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Ritonga, Budiman, Kadek Deddy Ariyanta, and I. Made Darmajaya. "Management mature sacrococcygeal teratoma: a case report." International Journal of Research in Medical Sciences 7, no. 10 (2019): 3891. http://dx.doi.org/10.18203/2320-6012.ijrms20194195.

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Mature sacrococcygeal teratoma (SCT) are uncommon neoplasm comprised of mixed elements derived from three germ layers. They attract attention because of their gross appearance and bizarre histology. Tumor of the sacrococcygeal region, referred to as sacrococcygeal teratomas (SCTs) in most reports, generally present in two distinct fashions: neonates with large predominately external lesions, which are detected in utero or at birth and are rarely malignant; and older infants and children who present with primarily hidden pelvic tumors with a much higher rate of malignancy. Sacrococcygeal terato

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Saha, Laxmi, Ola Haidar Wahbi, Evelio Alberto Ramos, Yasmin Abozenah, Maha Ghorabah, and Martin Corbally. "Case Report of a Rapidly Growing Sacrococcygeal Teratoma: A Planned Preterm Cesarean Delivery May Improve Fetal Outcome." Journal of the Bahrain Medical Society 34, no. 2 (2022): 57–61. http://dx.doi.org/10.26715/jbms.34_2022_2_9.

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Sacrococcygeal teratoma (SCT) is the most commonly diagnosed congenital tumor during the neonatal period. The outcome of SCT is dependent on the growth rate, the presence of solid components in cancer, and the presence or absence of high flow cardiac involvement of the fetus. This case report presents the management and outcome of a pregnant woman carrying a fetus with a rapidly growing SCT. Confirmation of diagnosis was based on the universal prenatal ultrasound examination standards. Eventually, the patient delivered a girl weighing 2.9 kg, including the neoplasm, by a planned Cesarean secti

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Cui, Shengjie, Jing Han, Binny Khandakar, et al. "Recurrent Adult Sacrococcygeal Teratoma Developing Adenocarcinoma: A Case Report and Review of Literatures." Case Reports in Pathology 2021 (November 27, 2021): 1–6. http://dx.doi.org/10.1155/2021/5045250.

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Sacrococcygeal teratomas (SCT) are most commonly seen in infants and children but are rare in adults. Most adult SCT are benign and mature with a minority of tumors having immature components or overt malignancy. Here, we report a 65-year-old female with a SCT developing adenocarcinoma. The patient was diagnosed with benign sacrococcygeal cystic teratoma on her initial hospital visit and was treated with surgical resection. She was followed up postoperatively and was noted to have a markedly elevated CA 19-9 level 13 months after the surgery. Radiological and clinical examination revealed thic

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Conference papers on the topic "Sacrococcygeal teratoma(SCT)"

1

Al-Kaisi, N., K. Weiler, D. Geiger, et al. "Frühgeburt bei Sacrococcygealem Teratom (SCT)." In 28. Deutscher Kongress für Perinatale Medizin. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1607793.

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