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Hooshmand, Sara

https://orcid.org/0000-0001-7826-4362

Mayo Clinic

Mayo Clinic

Citations 9

The Role of Trendelenburg Positioning for the Acute Symptomatic Management of Spontaneous Intracranial Hypotension
Zhang, Tony , Hooshmand, Sara , Rogers, Nathaniel , Sohutskay, David O , Toledano, Michel , Stitt, Derek , Carabenciov, Ivan D. , Cutsforth‐Gregory, Jeremy K. , Mustafa, Rafid , Hooshmand, Sara J , Rogers, Nathaniel P , Stitt, Derek W, Mustafa, Rafid , Madhavan, Ajay A.

The Neurohospitalist | November 17, 2025 | Volume: 16 | Issue: 3 | Pages: 280-285

10.1177/19418744251399726 Get It

Background Spontaneous intracranial hypotension (SIH) results from cerebrospinal fluid (CSF) leakage due to spinal dural tears or CSF–venous fistulas. Orthostatic headache is the hallmark presentation, though severe downward displacement of the brainstem may lead to altered consciousness or coma. Definitive treatments include targeted epidural blood patches, venous embolization, or surgical repair. Methods This article reviews the role of the Trendelenburg position as a temporizing measure in the acute management of SIH. We describe the correct technique, physiologic rationale, and practical considerations for its application, with attention to both therapeutic and diagnostic utility. Discussion Positioning the patient with the feet elevated above the head can reduce brain sag and provide short-term symptomatic relief while awaiting definitive treatment. Although the Trendelenburg position is widely used in practice, supporting evidence remains limited, and clinicians must be aware of its benefits, indications, and inherent limitations. Its appropriate application may assist in stabilizing patients with acute or severe SIH, particularly those with impaired consciousness, until more definitive interventions are pursued.
Application of the ADEM definition to cerebral attacks of MOG antibody-associated disease
Hooshmand, Sara , Vorasoot, Nisa , Li, Xiaoyang , Chen, John J. , Redenbaugh, Vyanka , Valencia-Sánchez, Cristina , López‐Chiriboga, A. Sebastian , Sechi, Elia , Tillema, Jan‐Mendelt , Tajfirouz, Deena , Tisavipat, Nanthaya , Guo, Kai , Hooshmand, Sara J , Banks, Samantha A. , Valencia Sanchez, Cristina , Lopez-Chiriboga, A Sebastian , Sechi, Elia , Basso, Michael, Tisavipat, Nanthaya , Flanagan, E P , Chen, John J , Vorasoot, Nisa , Li, Xiaoyang, Cacciaguerra, Laura , Basso, Michael R. , Hardy, Todd A. , Pittock, Sean J. , Flanagan, Eoin P.

Multiple Sclerosis Journal | August 19, 2025 | Volume: 31 | Issue: 14 | Pages: 1629-1640

10.1177/13524585251359450 Get It

Background: Acute disseminated encephalomyelitis (ADEM) is a demyelinating syndrome observed in myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) but there are limited data on application of this definition to its cerebral attacks or in adults with this disease. Methods: We analyzed patients from the Mayo Clinic MOGAD cohort ( n = 263) with cerebral attacks. We assessed whether children (<18 years-old) and adults (⩾18 years-old) fulfilled the 2013 ADEM definition. Results: We identified 89 patients (children, 34; adults, 55) and 55/89 (62%) were of female sex. Acute magnetic resonance imaging (MRI) abnormalities included: poorly demarcated T2 lesions (white matter, 85 (96%); deep gray matter, 41 (46%); T1-hypointense lesions (42 (47%)). Forty-two patients did not fulfill the ADEM definition due to: monofocal syndrome, 9; or no encephalopathy, 33. The remaining 47 patients (53%: children, 27/34 (79%); adults, 20/55 (36%)) fulfilled the ADEM definition, and 14 had preceding attacks, and 34 had subsequent attacks relative to ADEM episode. The features in children and adults with ADEM were broadly comparable. Conclusion: Applying the ADEM definition to MOGAD cerebral attacks highlighted that an update of the 2013 ADEM definition would be beneficial and could explicitly state its application to both adults and children and allow it to be applied to attacks at any time during the disease course.
Teaching NeuroImage: Female Hormonal Therapy and Cerebral Cavernous Malformation Hemorrhage
Hooshmand, Sara , Flemming, Kelly D. , Hooshmand, Sara J , Flemming, Kelly D

Neurology | August 14, 2025 | Volume: 105 | Issue: 5 | Pages: No page available

10.1212/wnl.0000000000214081 Get It

A 61-Year-Old Woman with Unresponsiveness and Abnormal Movements (P10-7.006)
Alexandres, Christina, Hooshmand, Sara , Rabinstein, Alejandro A.

Neurology | April 7, 2025 | Volume: 104 | Issue: 7_Supplement_1 | Pages: No page available

10.1212/wnl.0000000000210338 Get It

Trendelenburg Reversal of Coma in Spontaneous Intracranial Hypotension (P7-3.002)
Rogers, Nathaniel , Sohutskay, David O , Toledano, Michel , Cutsforth‐Gregory, Jeremy K. , Zhang, Tony , Hooshmand, Sara , Mustafa, Rafid

Neurology | April 7, 2025 | Volume: 104 | Issue: 7_Supplement_1 | Pages: No page available

10.1212/wnl.0000000000210364 Get It

Teaching Video NeuroImage: Isolated Presentation of Cavernous Sinus Syndrome From CNS Lymphoma
Itoh, Christopher Y. , Griffin, Kim J. , Yi, Dongni , Hooshmand, Sara , Webb, Lauren M. , Giannini, Caterina , Graff‐Radford, Jonathan , Mustafa, Rafid , Hooshmand, Sara J , Giannini, Caterina , Mustafa, Rafid , Itoh, Christopher Yuki

Neurology | August 23, 2024 | Volume: 103 | Issue: 6 | Pages: No page available

10.1212/wnl.0000000000209767 Get It

BRAT1 Associated Leukodystrophy exacerbated by Lymphoma directed Chemotherapy (P13-9.005)
Ruff, Michael W. , Hooshmand, Sara , Chohan, Karan

Neurology | December 6, 2023 | Volume: 98 | Issue: 18_supplement | Pages: No page available

10.1212/wnl.98.18_supplement.136 Get It

BRAT1-Associated Leukodystrophy Exacerbated by Classic Hodgkin Lymphoma–Directed Therapy
Hooshmand, Sara , Chohan, Karan , Renaud, Deborah L. , Ruff, Michael W. , Chohan, Karan L , Hooshmand, Sara J , Raghunathan, Aditya

The Neurologist | November 29, 2023 | Volume: 29 | Issue: 3 | Pages: 170-172

10.1097/nrl.0000000000000539 Get It

Introduction: BRCA1-associated ataxia-telangiectasia–mutated activator-1 (BRAT1) is responsible for cell cycle surveillance and mitochondrial function. The implications of adult-onset BRAT1-variant and the resulting phenotypic neurocognitive and imaging features have not been previously described. Case Report: A 66-year-old man with a recent diagnosis of classic Hodgkin lymphoma was referred to neuro-oncology for cognitive and motor decline, and progressive cerebral white matter changes noted on magnetic resonance imaging (MRI). A neurological examination revealed global weakness, broad-based gait, and bilateral extensor plantar responses. Brain MRI demonstrated periventricular, deep, and subcortical white matter T2/FLAIR hyperintensities without contrast enhancement. Cerebral spinal fluid studies were unremarkable. A GeneDX genetic leukodystrophy panel conduction revealed a pathogenic variant (c.294dupA; p.L99TfsX92) resulting in a truncated protein of BRAT1, along with a variant of uncertain significance (c.746A>G;p.E249G). A presumptive diagnosis of late-onset leukoencephalopathy secondary to the BRAT1 variant was made. In an attempt to combat his mitochondrial dysfunction, he was initiated on a mitochondrial cocktail, including B-100 complex and coenzyme Q10. He began lymphoma-directed combination chemotherapy and developed precipitous functional decline after 2 cycles of therapy. Compared with prechemotherapy imaging, repeat positron emission tomography/computed tomography metabolic imaging showed a response after 3 cycles of chemotherapy; however, repeat brain MRI showed worsening diffuse white matter hyperintensities and cerebral atrophy. Conclusion: Given the variability in phenotypes and clinical onset, leukodystrophies can be a diagnostic challenge. This case demonstrated progressive BRAT1-associated leukodystrophy exacerbated by chemotherapy-induced toxic leukoencephalopathy. Mitochondrial energy deficiency in the context of multiple metabolic insults was likely underlying the progressive neurological decline observed in this case of genetic leukodystrophy.
Teaching Video NeuroImage: Response to IVIg in a Patient With Steroid-Refractory Immune Checkpoint Inhibitor–Related Ocular Myopathy
Hooshmand, Sara , Pinto, Catarina Aragon , Pinto, Marcus Vinícius , Hooshmand, Sara J , Aragon Pinto, Catarina , Liewluck, T , Pinto, Marcus V , Liewluck, Teerin

Neurology | October 3, 2023 | Volume: 101 | Issue: 21 | Pages: No page available

10.1212/wnl.0000000000207864 Get It