scholarly journals Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review

BMC Neurology ◽  
2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Junyang Wang ◽  
Ming Liu ◽  
Wenjie Shang ◽  
Zhongqin Chen ◽  
Guoping Peng
2020 ◽  
Vol 6 ◽  
pp. 2513826X1989883
Author(s):  
Sarah L. Zhu ◽  
David Choi ◽  
Jenny Santos ◽  
Bernard S. Jackson ◽  
Matthew McRae

This is the first report of pilomatrix carcinoma in a man with C282Y myotonic dystrophy type 1. This pilomatrix carcinoma had originally presented as a rapidly growing recurrence of a histopathologically confirmed pilomatrixoma, removed a year prior. On examination, the fungating mass had measured 10 × 23 cm. A wide local resection with removal of suspicious lymph nodes was preformed, and the resulting defect was reconstructed with a latissimus dorsi myocutaneous flap and skin graft. Histologic investigation of the excised mass confirmed the diagnosis of pilomatrix carcinoma. This is the first reported case of pilomatrix carcinoma in a patient with a genetic condition that often presents with scalp pilomatrixomas. Potential implications of myotonic dystrophy on developing pilomatrix carcinoma are discussed.


2018 ◽  
Vol 46 (1) ◽  
pp. 72-74 ◽  
Author(s):  
Lleimi Alarcón-Pérez ◽  
Cristina Pastor-Laín ◽  
Lourdes Barragán-González ◽  
Claudia Sarrais-Polo ◽  
María T. López-Gil ◽  
...  

2012 ◽  
Vol 7 (4) ◽  
pp. 190-192
Author(s):  
Andres Silva-Rojas ◽  
Antonio Ysunza ◽  
Daniel Diaz-Torres ◽  
Mercedes Bardales-Lazcano ◽  
Maria C. Pamplona

2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Saya Iida ◽  
Hiroko Seino ◽  
Fumiko Nagahata ◽  
Soichiro Tatsuo ◽  
Sho Maruyama ◽  
...  

Abstract Background Cerebral ventriculomegaly is an abnormal feature characteristic of myotonic dystrophy type 1 (DM1). This retrospective study investigated the morphologic changes accompanied by ventriculomegaly in DM1 on brain MRI. Methods One hundred and twelve adult patients with DM1 and 50 sex- and age-matched controls were assessed. The imaging characteristics for evaluations included the z-Evans Index (ventriculomegaly), callosal angle (CA), enlarged perivascular spaces in the centrum semiovale (CS-EPVS), temporo-polar white matter lesion (WML) on 3D fluid-attenuated inversion recovery (FLAIR), disproportionately enlarged subarachnoid-space hydrocephalus (DESH), and pathological brain atrophy. The “z-Evans Index” was defined as the maximum z-axial length of the frontal horns to the maximum cranial z-axial length. To determine the imaging characteristics and genetic information (CTG repeat numbers) that were associated with the z-Evans Index, we used binominal logistic regression analyses. Results The z-Evans Index was significantly larger in the patients than in the controls (0.30 ± 0.05 vs. 0.24 ± 0.02; p < 0.01). The z-Evans Index was independently associated with the callosal angle (p < 0.01) and pathological brain atrophy (p < 0.01) but not with age, gender, CTG repeat numbers, or CS-EPVS. Of the 34 patients older than 49 years, 7 (20.6%) were considered to have DESH. Conclusions Our MRI study revealed a normal pressure hydrocephalus (NPH)-like appearance as a morphologic finding accompanied by ventriculomegaly in DM1 that tends to occur in elderly patients.


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