Literature DB >> 27341041

Epstein-Barr virus-associated smooth muscle tumor of the cavernous sinus: a delayed complication of allogenic peripheral blood stem cell transplantation: case report.

Amol Raheja1, Aleksandra Sowder2, Cheryl Palmer2, Fausto J Rodriguez3, William T Couldwell1.   

Abstract

Epstein-Barr virus (EBV)-associated smooth muscle tumors (SMTs) have recently been associated with primary and secondary immunodeficiencies. They are broadly divided into 3 subgroups: HIV-related, posttransplant, and congenital immunodeficiency. Subsequent to organ transplantation and acquired immunosuppression, a few cases of EBV-associated SMTs have been described in the liver, respiratory tract, and gastrointestinal system. To the authors' knowledge, intracranial involvement after peripheral blood stem cell transplantation has never been reported previously. The authors describe the case of a 65-year-old woman who presented with recent-onset painful ophthalmoplegia. She had a prior history of acute myelogenous leukemia requiring allogenic peripheral blood stem cell transplantation 2 years earlier, but she was in a remission phase. Imaging revealed a T1/T2 isointense, homogeneously enhancing lesion of the left cavernous sinus. A presumptive diagnosis of Tolosa-Hunt syndrome was made, and she was treated with steroids; however, her symptoms progressed quickly and repeat imaging revealed that the lesion was growing. To rule out leukemic deposits, a minimally invasive lateral orbitotomy extradural transcavernous approach was performed for biopsy sampling and debulking of the lesion. The biopsied tumor tissue was found to be infiltrative, grayish, firm, and moderately vascular. The final pathology results indicated an EBV-associated SMT of the cavernous sinus. Subsequently, the patient's steroid treatment was stopped and she had obtained partial symptomatic relief at her last follow-up visit, 3 months after surgery. EBV-associated SMT should be included in the differential diagnosis for intracranial and dural-based central nervous system lesions, especially in immunocompromised patients. Paradoxical response to steroids with worsening of symptoms is a hallmark of EBV-associated SMTs.

Entities:  

Keywords:  EBER = EBV-encoded small RNA; EBV = Epstein-Barr virus; EBV-associated smooth muscle tumor; Epstein-Barr virus; ICA = internal carotid artery; LOET = lateral orbitotomy extradural transcavernous; PT-SMT = posttransplantation SMT; SMA = smooth muscle actin; SMT = smooth muscle tumor; THS = Tolosa-Hunt syndrome; cavernous sinus; lateral orbitotomy extradural transcavernous approach; minimally invasive biopsy; oncology; peripheral blood stem cell transplantation

Mesh:

Year:  2016        PMID: 27341041     DOI: 10.3171/2016.4.JNS16290

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  4 in total

Review 1.  Tolosa-Hunt Syndrome: A Review of Diagnostic Criteria and Unresolved Issues.

Authors:  Paromita Dutta; Kamlesh Anand
Journal:  J Curr Ophthalmol       Date:  2021-07-05

Review 2.  Primary intracranial smooth muscle tumor associated with Epstein-Barr virus in immunosuppressed children: two cases report and review of literature.

Authors:  Maximiliano Paez-Nova; Karem Andaur; Ezequiel García-Ballestas; Diego Bustos-Salazar; Luis Rafael Moscote-Salazar; Osvaldo Koller; Sergio Valenzuela
Journal:  Childs Nerv Syst       Date:  2021-04-22       Impact factor: 1.475

3.  Multifocal EBV-associated smooth muscle tumors in a patient with cytomegalovirus infection after liver transplantation: a case report from Shiraz, Iran.

Authors:  Mohammad Hossein Anbardar; Neda Soleimani; Dornaz Safavi; Ahad Eshraghian; Abbas Ayoub
Journal:  Diagn Pathol       Date:  2022-01-07       Impact factor: 2.644

4.  Epstein-Barr virus associated hepatic smooth muscle tumor in a patient with acquired immunodeficiency syndrome: A case report.

Authors:  Qihui Zhou; Fengtian Wu; Yongzheng Guo; Biao Zhu
Journal:  Medicine (Baltimore)       Date:  2020-05       Impact factor: 1.817

  4 in total

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