Kaposiform hemangioendothelioma in tonsil of a child associated with cervical lymphangioma: a rare case report
2011

Rare Case of Kaposiform Hemangioendothelioma in a Child's Tonsil

Sample size: 1 publication Evidence: low

Author Information

Author(s): Rekhi Bharat, Sethi Shweta, Kulkarni Suyash S, Jambhekar Nirmala A

Primary Institution: Tata Memorial Hospital, Parel, Mumbai

Conclusion

This case highlights a rare occurrence of Kaposiform hemangioendothelioma in the tonsil of a child, associated with neck lymphangioma but not with Kasabach-Merritt phenomenon.

Supporting Evidence

  • Kaposiform hemangioendothelioma is a rare vascular tumor usually found in infants.
  • This case is the second documented instance of KHE in the tonsil.
  • The tumor was associated with a neck lymphangioma but not with the life-threatening Kasabach-Merritt phenomenon.

Takeaway

A 2-year-old boy had a rare tumor in his tonsil that is usually found in other parts of the body, and it was linked to another condition in his neck.

Methodology

The case involved clinical diagnosis, imaging studies, and histopathological examination of the excised tonsillar mass.

Limitations

The status of resection margins could not be commented upon due to incomplete submission of sections.

Participant Demographics

A 2-year-old male child.

Digital Object Identifier (DOI)

10.1186/1477-7819-9-57

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