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6 "Myopathy"
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Case reports
Predominant Myofibrillar Pathology with Preserved Sarcolemmal Aquaporin 4 Immunoreactivity in a Patient with Neuromyelitis Optica-Associated HyperCKemia
So-Young Huh, Jin-Hong Shin, Yeong-Eun Park, Ho Jin Kim, Dae-Seong Kim
Kosin Med J. 2021;36(2):206-210.   Published online December 31, 2021
DOI: https://doi.org/10.7180/kmj.2021.36.2.206
  • 2,467 View
  • 8 Download
Abstract PDFPubReader   ePub   

A 49-year-old man developed recurrent myalgia and hyperCKemia during acute attacks of neuromyelitis optica. Muscle biopsy was performed, and the pathological findings were analyzed. Predominant myofibrillar pathology was observed, which constitutes a unique finding that has not been reported before. This case result shows that neuromyelitis optica-associated hyperCKemia can produce variable pathologic phenotypes. Further studies are needed to elucidate the relationship between myofibril destruction and aquaporin 4 autoimmunity.

General Anesthesia for a Patient with GNE Myopathy: a case report
Christine Kang, Ji-hye An, Jae-Young Kwon, Boo-Young Hwang
Kosin Med J. 2020;35(1):64-68.   Published online June 30, 2020
DOI: https://doi.org/10.7180/kmj.2020.35.1.64
  • 3,169 View
  • 22 Download
Abstract PDFPubReader   ePub   

GNE, or bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, myopathy presents with symptoms of foot drop, followed by lower and upper extremity muscle weaknesses and sparing of the quadriceps. Myopathies usually increase the risks of complications related to general anesthesia. The anesthetic management of patients with GNEmyopathy has not been previously reported. Herein, we report a case of GNEmyopathy in a 37-year-old woman and discuss anesthetic considerations for elective laparoscopic hysterectomy and bilateral salpingectomy, focusing on the postoperative airway management. We avoided administering neuromuscular-blocking agents and instead used a laryngeal mask airway.

The anesthetic management combining the use of a laryngeal mask airway and desflurane without neuromuscular-blocking agents provided sufficient abdominal and diaphragmatic muscle relaxations for sustaining the pneumoperitoneum for laparoscopic surgery.

Original article
The association between T wave inversion and apical hypertrophic cardiomyopathy
Cheol Byoung Chae, Ju Hee Ha, Jun Ho Kim, Jae Joon Lee, Han Il Choi, Ki Beom Park, Jin Hee Kim, Jung Hyun Choi
Kosin Med J. 2018;33(3):328-336.   Published online December 31, 2018
DOI: https://doi.org/10.7180/kmj.2018.33.3.328
  • 6,356 View
  • 16 Download
Abstract PDFPubReader   
Objectives

Electrocardiograhy (ECG) is the first step in hypertrophic cardiomyopathy (HCMP) diagnosis. For various reasons, the T wave inversion (TWI) and ECG change with time and HCMP is not easy to diagnosis. The aim of this retrospective study was to investigate the association between TWI on ECG and apical HCMP.

Methods

A total of 4,730 ECGs presenting TWI from January 2011 to March 2013 in Pusan National University Hospital were enrolled. 133 patients who were examined by both echocardiography and coronary angiogram were analyzed. Patients were divided into two groups: Group A (TWI ≥ 10 mm) and Group B (5 mm ≤ TWI < 10 mm). HCMP is defined by a wall thickness ≥ 15mm in one or more LV myocardial segments. Apical HCMP is defined to be hypertrophy that is confined to LV apex. The patients who had ECGs with at least one month interval were divided 3 groups: Normal T wave, Abnormal T wave, and Persistent TWI. The prevalence of Apical HCMP and coronary artery disease (CAD) was reviewed among the three groups.

Results

In this study there were a total 133 patients, with patients divided into Group A which had 15 patients and Group B which had 118 patients. Among the 23 patients with apical HCMP, three patients were Group A and twenty patients were Group B (P = 0.769). Regarding constancy of TWI, persistent TWI group was higher in apical HCMP than in other groups (P = 0.038). CAD had no difference between groups (P = 0.889).

Conclusions

T wave negativity was not associated with incidence of apical HCMP. However, apical HCMP was diagnosed more frequently in patients with persistent TWI. Further follow up echocardiographic study is needed to evaluate the progression of apical HCMP in patients with TWI.

Case reports
Recurrent fetal postpartum stress induced cardiomyopathy after normal vaginal delivery
Yong-Sun Noh, Sung-Ho Her, Jong Bum Kwon, Chan Joon Kim, Tae-Seok Kim
Kosin Med J. 2017;32(2):244-250.   Published online December 29, 2017
DOI: https://doi.org/10.7180/kmj.2017.32.2.244
  • 3,537 View
  • 5 Download
  • 1 Citations
Abstract PDFPubReader   ePub   

Stress induced cardiomyopathy is a disease that shows a dysfunction of the ventricle, but it can be rapidly reversible. It often occurs in older women primarily who suffers from emotional or physical stress. There are some case reports about postpartum stress induced cardiomyopathy. Most of the patients are recovered naturally within days to weeks. We report a case of a 37 years-old woman, who had experienced postpartum stress induced cardiomyopathy 8 years ago, revisited hospital because of cardiomyopathy after secondary delivery. Herein we report a rare case of recurrent stress induced cardiomyopathy after secondary normal vaginal delivery.

Citations

Citations to this article as recorded by  
  • Takotsubo Cardiomyopathy in Pregnancy: A Focused Review
    Heena Garg, Shashi Singh, Rashmi Ramachandran, Anjan Trikha
    Journal of Obstetric Anaesthesia and Critical Care.2023; 13(2): 142.     CrossRef
A Case of Cardiac Arrest due to Multivessel, Diffuse Coronary Spasm in Moyamoya Disease
Young Min Choi, Jung Woo Choi, Dong Ho Kang, Choong Hwan Kwak, Jin Yong Hwang, Jin Sin Koh
Kosin Med J. 2017;32(1):111-117.   Published online January 19, 2017
DOI: https://doi.org/10.7180/kmj.2017.32.1.111
  • 2,418 View
  • 6 Download
Abstract PDFPubReader   ePub   

Moyamoya disease is characterized by progressive stenosis of the distal portion of the internal carotid arteries and fragile collateral vessels in the brain. The precise pathogenesis is still not known. Although extracranial vessel involvement is very rare, coronary arterial involvement has recently been reported. Here, we report a case of diffuse, multivessel coronary spasm leading to cardiac arrest and myocardial infarction in a 47-year-old man with moyamoya disease with no underlying emotional or physical stress.

A Case of Stress Induced Cardiomyopathy in 28 Years Old Female after Epinephrine Local Injection
Ju Kyeon Yim, Sung Dong Kwak, Jae Young Park, Jae Hong Cheon, Sung Yul Choi, Tae Joon Cha, Joon Sang Lee
Kosin Med J. 2009;24(1):164-168.   Published online June 30, 2009
  • 640 View
  • 1 Download
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