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Krecke, Karl N.

https://orcid.org/0000-0003-1950-5589

Mayo Clinic

Mayo Clinic

Citations 61

Short Myelitis Lesions in Aquaporin-4-IgG-positive Neuromyelitis Optica Spectrum Disorders (S46.005)
Krecke, Karl N. , Lennon, Vanda A. , Lucchinetti, Claudia F. , Wingerchuk, Dean M. , Shuster, Elizabeth A., Jiao, Yujuan , Horta, Erika , Flanagan, Eoin P. , Weinshenker, Brian G. , McKeon, Andrew , Pittock, Sean J.

Neurology | December 6, 2023 | Volume: 84 | Issue: 14_supplement | Pages: No page available

10.1212/wnl.84.14_supplement.s46.005 Get It

Limited resection preserved verbal memory outcome in drug-resistant dominant temporal lobe epilepsy due to temporal encephaloceles (S24.002)
Smith, Kelsey , Alden, Eva , Kanth, Kiran , Krecke, Karl N. , Witte, Robert J. , So, Elson, Cascino, Gregory D. , Smith, Kelsey, Gompel, Jamie J. Van , So, Elson L., Britton, Jeffrey W. , Wong‐Kisiel, Lily C.

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

10.1212/wnl.98.18_supplement.1735 Get It

Development of new or enlarging MRI lesions outside of attacks is rare in myelin oligodendrocyte glycoprotein antibody-associated disease (S3.004)
Chen, John , Morris, Pearse , Krecke, Karl N. , Tillema, Jan‐Mendelt , López‐Chiriboga, A. Sebastian , Lucchinetti, Claudia F. , Zalewski, Nicholas L. , Bhatti, Muhammad Tariq , Syc‐Mazurek, Stephanie B. , Sechi, Elia , Messina, Steven A. , Buciuc, Marina , Pittock, Sean J. , Flanagan, Eoin P.

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

10.1212/wnl.98.18_supplement.1680 Get It

EEG Source Localization in Temporal Encephaloceles: Concordance With Surgical Resection and Clinical Outcomes
Cox, Benjamin C. , Kanth, Kiran , Krecke, Karl N. , Witte, Robert J. , Brinkmann, Benjamin H. , Agashe, Shruti H, Wong-Kisiel, Lily C. , Brinkmann, Benjamin H , Agashe, Shruti , Smith, Kelsey M. , Gompel, Jamie J. Van , Wong‐Kisiel, Lily C.

Journal of Clinical Neurophysiology | September 27, 2023 | Volume: 41 | Issue: 6 | Pages: 515-521

10.1097/wnp.0000000000001021 Get It

Purpose: Temporal encephaloceles are a cause of drug-resistant temporal lobe epilepsy; however, their relationship with epileptogenesis is unclear, and optimal surgical resection is uncertain. EEG source localization (ESL) may guide surgical decision-making. Methods: We reviewed patients at Mayo Clinic Rochester with drug-resistant temporal lobe epilepsy and temporal encephaloceles, who underwent limited resection and had 1-year outcomes. EEG source localization was performed using standard density scalp EEG of ictal and interictal activity. Distance from dipole and standardized low-resolution brain electromagnetic tomography (sLORETA) solutions to the encephalocele were measured. Concordance of ESL with encephalocele and surgical resection was compared with 1-year surgical outcomes. Results: Seventeen patients met criteria. The mean distances from ESL results to encephalocele center for dipole and sLORETA analyses were 23 mm (SD 9) and 22 mm (SD 11), respectively. Ten patients (55.6%) had Engel I outcomes at 1 year. Dipole-encephalocele distance and sLORETA-encephalocele distance were significantly longer in patients with Engel I outcome and patients whose encephalocele was contained by sLORETA had worse outcome as well; however, multiple logistic regression analysis found that only containment of encephalocele by the sLORETA current density was significant (P < 0.05), odds ratio 0.12 (95% confidence interval [0.021, 0.71]). Conclusions: EEG source localization of scalp EEG localizes near encephaloceles, however, typically not in the encephalocele itself; this may be due to scalp EEG sampling propagated activity or alternatively that the seizure onset zone extends beyond the herniated cortex. Surprisingly, we observed increased ESL to encephalocele distances in patients with excellent surgical outcomes. Larger cohort studies including intracranial EEG data are needed to further explore this finding.
Hemicord White Matter Enhancement and the Croissant Sign in Cervical Spondylotic Myelopathy
Li, Xiaoyang , Krecke, Karl N. , Weinshenker, Brian G. , Ζεκερίδου, Αναστασία , Toledano, Michel , Weinshenker, Brian G , Clarke, Michelle J. , Flanagan, Eoin P.

Neurology | August 30, 2023 | Volume: 101 | Issue: 21 | Pages: 968-969

10.1212/wnl.0000000000207793 Get It

Pituitary volume changes in pregnancy and the post-partum period
Benson, John C. , Malyuk, David F. , Madhavan, Ajay A. , Krecke, Karl N. , Little, Jason T. , Passe, Theodore J. , Lindell, E. Paul , Eckel, Laurence J. , Madhavan, Ajay A , DeLone, David R. , Lindell, Edward P, Benson, John , Guérin, J.

The Neuroradiology Journal | August 17, 2023 | Volume: 37 | Issue: 1 | Pages: 39-42

10.1177/19714009231196470 Get It

Purpose Imaging changes in the pituitary volume during pregnancy remains scantly researched. This study set out to assess the differences in total, anterior, and posterior pituitary volume in pregnant women compared to nulliparous and post-partum women. Materials and Methods A retrospective review was completed of women that had undergone MRI imaging of the brain. Patients were divided into three cohorts: pregnant, nulliparous, and post-partum (defined as being within 12 months of delivery). Anterior and posterior pituitary volumes were manually measured. Results 171 patients were included, of which 68 were pregnant, 52 were post-partum, and 51 were nulliparous. The average anterior (621.0 ± 171.6 mm 3 ) and total (705.4 ± 172.2 mm 3 ) pituitary volumes were significantly larger in pregnant patients than nulliparous women (522.6 ± 159.8 mm 3 and 624.5 ± 163.7 mm 3 , respectively) ( p = .002 and p = .01, respectively). The posterior pituitary volume was significantly smaller in pregnant women (84.4 ± 32.9 mm 3 ) compared to both post-partum (101.2 ± 42.0 mm 3 ) and nulliparous (102.0 ± 46.1 mm 3 ) women ( p = .02 for both). Conclusions The anterior and total pituitary volumes are significantly larger during pregnancy persisting into the post-partum period. The posterior pituitary volume, conversely, decreases during pregnancy, and returns to its normal size in the post-partum period.
Cerebral Cortical Encephalitis in Myelin Oligodendrocyte Glycoprotein Antibody‐Associated Disease
Guo, Yong , Krecke, Karl N. , Chen, John J. , Redenbaugh, Vyanka , Montalvo, Mayra , Elsbernd, Paul , Tillema, Jan‐Mendelt , López‐Chiriboga, A. Sebastian , Budhram, Adrian , Kunchok, Amy , Dubey, Divyanshu , Pittock, Sean J. , Lucchinetti, Claudia F. , Dubey, Divyanshu , Valencia-Sánchez, Cristina , Pittock, S J , Flanagan, E P , Lopez-Chiriboga, A Sebastian , Budhram, Adrian , Dubey, Divyanshu , Pittock, Sean J , Chen, John J , Dubey, Divyanshu , Valencia Sanchez, Cristina , Sechi, Elia , Flanagan, Eoin P.

Annals of Neurology | November 14, 2022 | Volume: 93 | Issue: 2 | Pages: 297-302

10.1002/ana.26549 Get It

Cerebral cortical encephalitis (CCE) is a recently described myelin oligodendrocyte glycoprotein antibody‐associated disease (MOGAD) phenotype. In this observational retrospective study, we characterized 19 CCE patients (6.7% of our MOGAD cohort). Headache (n = 15, 79%), seizures (n = 13, 68%), and encephalopathy (n = 12, 63%) were frequent. Magnetic resonance imaging revealed unilateral (n = 12, 63%) or bilateral (n = 7, 37%) cortical T2 hyperintensity and leptomeningeal enhancement (n = 17, 89%). N‐Methyl‐D‐aspartate receptor autoantibodies coexisted in 2 of 15 tested (13%). CCE pathology (n = 2) showed extensive subpial cortical demyelination (n = 2), microglial reactivity (n = 2), and inflammatory infiltrates (perivascular, n = 1; meningeal, n = 1). Most received high‐dose steroids (n = 17, 89%), and all improved, but 3 had CCE relapses. This study highlights the CCE spectrum and provides insight into its pathogenesis. ANN NEUROL 2023;93:297–302