IMMUNE THROMBOCYTOPENIC PURPURA AS A PREDECESSOR OF GLIOBLASTOMA MULTIFORME

Authors

  • Nicolas Rojas Stambuk Universidad del Valle, Bolivia
  • Ivanova Saavedra Tapia Hospital Obrero N°2–Caja Nacional de Salud

DOI:

https://doi.org/10.52428/20756208.v17i42.224

Keywords:

Glioblastoma, Purpura, Thrombocytopenia, Autoimmune

Abstract

The clinical case presented below is that of a 68-year-old female patient with a history of long-standing type 2 diabetes mellitus, who presented clinical symptoms characterized by aphasia, apraxia, and facio-brachio-crural hemiparesis on several occasions. These symptoms were attributed to subarachnoid hemorrhage due to severe thrombocytopenia. For this she was diagnosed with Immune Thrombocytopenic Purpura. She was hospitalized on several occasions during which complementary studies were carried out. These studies helped us diagnosed an autoimmune hepatitis. In her last hospitalization for the same condition, a simple cerebral computed tomography was performed due to the already known history of subarachnoid hemorrhage in which a lesion compatible with a solid mass was evidenced. The study of the tumor was completed with a magnetic resonance image (MRI) contrasted with gadolinium. In the MRI we observed an infiltrative tumor mass highly suggestive of a high-grade glial tumor (Multiform glioblastoma). Due to the characteristics of the patient´s underlying diseases and family decision, no treatment was carried out. This led to a decline in the general condition of the patient, culminating in her death.

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Author Biography

Ivanova Saavedra Tapia, Hospital Obrero N°2–Caja Nacional de Salud

Egresada de la Facultad de Medicina de la Universidad Mayor de San Simon. Realizó su especialidad en Hematología en el Hospital Ramón y Cajal de la ciudad de Madrid, España. 

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Published

2022-06-30

How to Cite

Rojas Stambuk, N., & Saavedra Tapia, I. . (2022). IMMUNE THROMBOCYTOPENIC PURPURA AS A PREDECESSOR OF GLIOBLASTOMA MULTIFORME. Revista De Investigación E Información En Salud, 17(42), 39–47. https://doi.org/10.52428/20756208.v17i42.224

Issue

Section

Case Report

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