Malignant Sacrococcygeal Teratoma with Yolk Sac Differentiation: A Rare Case Report

Authors

  • Sayeda Hoosne Harisha Department of Pathology, Gauhati Medical College and Hospital, Guwahati, Assam, India.
  • Manoj Barman Department of Pathology, Gauhati Medical College and Hospital, Guwahati, Assam, India
  • Jabin Musfique Department of Pathology, Gauhati Medical College and Hospital, Guwahati, Assam, India
  • Rajib Ray Baruah Department of Paediatric Surgery, Gauhati Medical College and Hospital, Guwahati, Assam, India
  • Manjula Choudhury Department of Pathology, Gauhati Medical College and Hospital, Guwahati, Assam, India

DOI:

https://doi.org/10.21276/apalm.3620

Keywords:

Sacrococcygeal teratoma, Yolk sac tumour, Neonate

Abstract

Sacrococcygeal teratomas (SCTs) are the most common germ cell tumours in neonates and infants, with malignant transformation often observed in postnatal cases. Yolk sac tumour (YST) is the most frequent malignant germ cell component seen in SCTs. We report a case of a 3-month-old infant presenting with a Type II SCT, showing histopathological features of yolk sac tumour differentiation.

References

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Published

30-07-2025

How to Cite

1.
Harisha SH, Barman M, Musfique J, Baruah RR, Choudhury M. Malignant Sacrococcygeal Teratoma with Yolk Sac Differentiation: A Rare Case Report. Ann of Pathol and Lab Med [Internet]. 2025 Jul. 30 [cited 2025 Dec. 5];12(7):C106-109. Available from: https://pacificejournals.com/journal/index.php/apalm/article/view/3620

Issue

Section

Case Report