Sacrococcygeal giant hemangiopericytoma: a rare presentation and management

Authors

  • Jose de Jesus Orozco Division of Plastic and Reconstructive Surgery, Dr. Manuel Gea Gonzalez General Hospital, México City, México
  • Enrique Vaca Perez Division of Oncology Surgery, Del Bajío General Hospital, Leon, México
  • Jose Eduardo Telich Tarriba Division of Plastic and Reconstructive Surgery, Dr. Manuel Gea Gonzalez General Hospital, México City, México
  • Enrique Chavez Serna Division of Plastic and Reconstructive Surgery, Dr. Manuel Gea Gonzalez General Hospital, México City, México
  • Enrique Velazquez Zabaleta Division of Plastic and Reconstructive Surgery, Dr. Manuel Gea Gonzalez General Hospital, México City, México
  • Heriberto Garza de la Llave Division of Plastic and Reconstructive Surgery, Dr. Manuel Gea Gonzalez General Hospital, México City, México
  • Antonio Ruiz Fernandez Division of Plastic and Reconstructive Surgery, Dr. Manuel Gea Gonzalez General Hospital, México City, México

DOI:

https://doi.org/10.18203/2320-6012.ijrms20192546

Keywords:

Endothelium, Hemangiopericytoma, Neoplasm, Reconstruction, Sacrococcygeal, Vascular

Abstract

Hemangiopericytoma is a tumor derivated from the mesenchymal cells that surround the capillary of blood vessels. It has a several anatomic localization and clinic scenarios, it´s presentation with a media in the 6th decade; an early diagnostic and treatment represents a better clinic scenario for the patient. The next article presents a case report of a 51 years old man with a tumor localized in the sacrococcygeal space, with big dimensions that limited his daily activities without other symptomatology, image studies with no evidence of distant progression. Surgical resection was performed, removing mass depending from mayor and minor gluteus, achieving an immediate reconstruction with a satisfactory aesthetic and functional result. The authors presented this rare case due to the lack of published information and how it can be treated to achieve good results.

References

Onokl T, Kanno H, Alzawa T, Hashimoto K, Itol E, Ozawa H. Recurrent Primary osseus hemangiopericitoma in the thoracic spine: a case report and literature review. Eur Spine J. 2018 Jul;27(Suppl 3):386-392

Damodaran O, Robbins P, Knuckey N, Bynevelt M, Wong G, Lee G. Primary intracranial haemangiopericytoma: comparison of survival outcomes and metastatic potential in WHO grade II and III variants. J Clin Neurosci. 2014;21(8):1310-4.

Zhang G, Zhang L, Li D, Wu Z, Zhang J. Analysis of prognostic factors, survival rates, and treatment in anaplastic hemangiopericytoma. World Neurosurg. 2017 Aug 1;104:795-801.

Lorigan J, David C, Evans H, Wallace S. The Clinical and Radiologicall Manifestatios of Hemangiopericytoma. AJR. 1989;153:345-9.

Enzinger FM, Smith BH. Hemangiopericytoma. An analysis of 106 cases. Hum Pathol. 1976;7:61-82.

Catalano PJ, Brandwein M, Shah DK, Urken ML, Lawson W, Biller HF. Sinonasal hemangiopericytomas: a clinicopathologic and immunohistochemical study of seven cases. Head Neck. 1996;18:42-53.

Stout AP, Murray MR. Hemangiopericytoma: vascular tumor featuring Zimmermans pericytes. Ann Surg. 1942;116:2633.

Fukunaga M, Shimoda T, Nikaido T, Ushigome S, Ishikawa E. Soft tissue vascular tumor. A flowcytometric DNA analysis. Cancer. 1993;71:2233-41.

Morandi U, Stefani A, De Santis M, Paci M, Lodi R. Preoperative embolization in surgical treatment of mediastinal hemangiopericytoma. Ann Thorac. Surg. 2000;69:937-9.

Damodaran O, Robbins P, Knuckey N, Bynevelt M, Wong G, Lee G. Primary intracranial haemangiopericytoma: comparison of survival outcomes and metastatic potential in WHO grade II and III variants. J Clin Neurosci. 2014;21(8):1310-4.

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Published

2019-05-29

How to Cite

Orozco, J. de J., Perez, E. V., Telich Tarriba, J. E., Serna, E. C., Zabaleta, E. V., de la Llave, H. G., & Fernandez, A. R. (2019). Sacrococcygeal giant hemangiopericytoma: a rare presentation and management. International Journal of Research in Medical Sciences, 7(6), 2445–2448. https://doi.org/10.18203/2320-6012.ijrms20192546

Issue

Section

Case Reports