Variant of Wellen's syndrome in type 1 diabetic patient: A case report

被引:0
作者
Obi, Mukosolu Florence [1 ]
Sharma, Manjari [1 ]
Namireddy, Vikhyath [2 ]
Gargiulo, Paul [1 ]
Noel, Chelsea [2 ]
Hyun, Cho [1 ]
De Gale, Blossom [2 ]
机构
[1] Wyckoff Hts Med Ctr, Internal Med, 374 Stockholm, Brooklyn, NY 11237 USA
[2] St Georges Univ, Sch Med, Clin Rotat, True Blue 96038, Grenada
来源
WORLD JOURNAL OF CARDIOLOGY | 2023年 / 15卷 / 09期
关键词
Wellens's syndrome; Biphasic T waves; Deeply inverted T waves; Precordial leads; Left anterior descending artery; Pseudo-normalization; Right coronary artery; Left circumflex artery; Case report;
D O I
10.4330/wjc.v15.i9.462
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Wellen's syndrome is a form of acute coronary syndrome associated with proximal left anterior descending artery (LAD) stenosis and characteristic electrocardiograph (ECG) patterns in pain free state. The abnormal ECG pattern is classified into type A (biphasic T waves) and type B (deeply inverted T waves), based on the T wave pattern seen in the pericodial chest leads. CASE SUMMARY We present the case of a 37-year-old male with history of type 1 diabetes mellitus (T1DM), gastroparesis, mild peripheral artery disease and right toe cellulitis on IV antibiotics who presented to the emergency department with nausea, vomiting and abdominal pain for 3 d and as a result couldn't take his insulin. Noted to have fasting blood sugar 392 mg/dL. Admitted for diabetic gastroparesis. During the hospital course, the patient was asymptomatic and denied any chest pain. On admission, No ECG and troponin draws were performed. On day 2, the patient became hypoxic with oxygen saturation 80% on room air, intermittent mild right-sided chest pain which he attributed to vomiting from his gastroparesis. Initial ECG done was significant for Biphasic T wave changes in leads V2 and V3 and elevated high sensitivity troponin. Patient was transitioned to cardiac intensive care unit and cardiac catheterization performed with result significant for extensive coronary artery disease. CONCLUSION This case highlights an exceptional manifestation of Wellen's syndrome, wherein the right coronary artery and circumflex artery display a remarkable 100% constriction, alongside a proximal LAD stenosis of 90%-95%. Notably, this occurrence transpired in a patient grappling with extensive complications arising from T1DM. Moreover, it underscores the utmost significance of promptly recognizing the presence of Wellen's syndrome and swiftly initiating appropriate medical intervention.
引用
收藏
页码:462 / 468
页数:7
相关论文
共 50 条
[21]   Carvajal Syndrome- A Variant of Naxos Disease: A Case Report [J].
Mandal, Krishna Deo ;
Shrestha, Pun Narayan ;
Ghimire, Anjila ;
Joshi, Prakash ;
Agrawal, Sumit ;
Shrestha, Prapti .
JOURNAL OF NEPAL MEDICAL ASSOCIATION, 2022, 60 (246) :187-191
[22]   Caroli syndrome in a patient with psoriasis: A case report [J].
Wang, Longfei ;
Ge, Yunjie ;
Zhang, Chuanhui ;
Jin, Zhenjing .
ASIAN JOURNAL OF SURGERY, 2023, 46 (02) :1105-1106
[23]   Keratoconus in a patient with Alport syndrome: A case report [J].
Majid Moshirfar ;
David F Skanchy ;
Aaron T Gomez ;
Yasmyne C Ronquillo ;
Benjamin Buckner ;
Phillip C Hoopes .
World Journal of Clinical Cases, 2019, (19) :3012-3017
[24]   PERCHING syndrome caused by variant gene KLHL7 in the first Iranian patient: a case report study [J].
Ghelichi-Ghojogh, Mousa ;
Golfiroozi, Saeed ;
Delavari, Sahar ;
Hosseini, Seyed Ahmad .
ANNALS OF MEDICINE AND SURGERY, 2024, 86 (02) :1048-1051
[25]   A Missense Mutation in LMX1A in a Patient With Moebius Syndrome: A Case Report [J].
Alnefaie, Ghaliah O. .
CUREUS JOURNAL OF MEDICAL SCIENCE, 2022, 14 (10)
[26]   Thoracic outlet syndrome in a patient with SAPHO syndrome - A case report [J].
Ohida, H. ;
Curuk, C. ;
Prescher, H. ;
Stegemann, E. ;
Burger, Th .
INTERNATIONAL JOURNAL OF SURGERY CASE REPORTS, 2021, 80
[27]   Case report: A novel COL3A1 variant in a Colombian patient with isolated cerebrovascular involvement in vascular Ehlers-Danlos syndrome [J].
Valencia-Cifuentes, Valeria ;
Sinisterra-Diaz, Stiven Ernesto ;
Quintana-Pena, Valentina ;
Folleco, Edgar ;
Nastasi-Catanese, Jose A. ;
Pachajoa, Harry ;
Fernandez-Cubillos, Juan P. .
FRONTIERS IN MEDICINE, 2024, 11
[28]   Case report: A rare case of pyruvate kinase deficiency and Crigler-Najjar syndrome type II with a novel pathogenic variant of PKLR and UGT1A1 mutation [J].
Wu, Huan ;
Wu, Long ;
Zhang, Quan ;
Zhang, Bao-fang .
FRONTIERS IN GENETICS, 2023, 14
[29]   Malignant anaplastic meningioma in neurofibromatosis type 1 patient: a rare case report [J].
AlAnsari, Ghada A. ;
Bukhari, Nedal ;
Abdulkader, Marwah M. ;
Alotain, Ibrahim ;
Taha, Mahmoud S. .
AME CASE REPORTS, 2022, 6
[30]   Malignant anaplastic meningioma in neurofibromatosis type 1 patient: a rare case report [J].
AlAnsari, Ghada A. ;
Bukhari, Nedal ;
Abdulkader, Marwah M. ;
Alotain, Ibrahim ;
Taha, Mahmoud S. .
AME CASE REPORTS, 2022, 6