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Methylphenidate-Induced Kleptomania in a Child with Down Syndrome 一例唐氏综合征患儿的哌甲酯诱发的盗窃性躁狂
Mathews journal of case reports Pub Date : 2023-01-01 DOI: 10.30654/mjcr.10082
Meltem Küçükdağ, H. N. Küçükdağ
{"title":"Methylphenidate-Induced Kleptomania in a Child with Down Syndrome","authors":"Meltem Küçükdağ, H. N. Küçükdağ","doi":"10.30654/mjcr.10082","DOIUrl":"https://doi.org/10.30654/mjcr.10082","url":null,"abstract":"Methylphenidate is the most preferred drug in the treatment of ADHD, which is one of the psychiatric diseases that often accompany Down’s syndrome. Methylphenidate, which is used safely in children and adolescents, may rarely show unexpected side effects. In our study, we present a case of kleptomania induced by methylphenidate in a child with Down syndrome, which resolved with the discontinuation of the drug","PeriodicalId":92691,"journal":{"name":"Mathews journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41655109","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Methylphenidate-Induced Henoch Schönleın Purpura: A Case Report 哌甲酯致过敏性紫癜1例报告
Mathews journal of case reports Pub Date : 2023-01-01 DOI: 10.30654/mjcr.10077
Meltem Küçükdağ, Nurcan Ünal
{"title":"Methylphenidate-Induced Henoch Schönleın Purpura: A Case Report","authors":"Meltem Küçükdağ, Nurcan Ünal","doi":"10.30654/mjcr.10077","DOIUrl":"https://doi.org/10.30654/mjcr.10077","url":null,"abstract":"","PeriodicalId":92691,"journal":{"name":"Mathews journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43772677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Assessed Breastfeeding Knowledge, Attitude, and Practice and Identified Associated Factors 评估母乳喂养的知识、态度和做法，并确定相关因素
Mathews journal of case reports Pub Date : 2022-12-30 DOI: 10.30654/mjcr.10081
Asma Hawasawi, N. Alhojaili, Hana Ahmed Al Bha
{"title":"Assessed Breastfeeding Knowledge, Attitude, and Practice and Identified Associated Factors","authors":"Asma Hawasawi, N. Alhojaili, Hana Ahmed Al Bha","doi":"10.30654/mjcr.10081","DOIUrl":"https://doi.org/10.30654/mjcr.10081","url":null,"abstract":"Assessment of Knowledge, Attitude and Practice of Breastfeeding and Associated Barriers, A Cross-Sectional Study in Maternal and Child Hospital Makkah, KSA, 2019. Background: Breastfeeding (BF) is now recognized worldwide to have great effects on both the mother and her baby. Method: This study was a descriptive cross-sectional hospital and community-based study. Conducted in Makkah for the community participants and Maternal and child hospital Makkah (MCHM). The study population comprised health care providers (HCP) and the women in MCHM and Makkah communities. A simple random technique was obtained to select 142 women. For the (HCP) we included all 31 HCPs in the hospital (total coverage). This study aimed to investigate the knowledge, attitude, and practice of breastfeeding and associated factors that affect compliance with breastfeeding among HCP and women in MCHM and Makkah community, KSA, 2019. Result: Most women get their knowledge about BF from family and a friend which gives chance to introduce wrong and untrusted information about BF and affects their attitudes and practices on BR. Generally, the knowledge about BR was good, while the attitude towards BR was negative towards BR (mainly from women from the community). Moreover, most of the participants agreed with all factors and barriers affecting BR. and there was a significant association between the knowledge and the attitude of the participants towards BF. Conclusion: There was a good chance to train and learn the required knowledge and practices of BR among the women even though they received full support to continue on BR and they are relatively younger and had high educational levels.","PeriodicalId":92691,"journal":{"name":"Mathews journal of case reports","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69531683","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Dangerous 'Mulberry' 危险的“桑树”
Mathews journal of case reports Pub Date : 2022-12-19 DOI: 10.30654/mjcr.10079
A. Chauhan, Devender Kumar Sharma
{"title":"The Dangerous 'Mulberry'","authors":"A. Chauhan, Devender Kumar Sharma","doi":"10.30654/mjcr.10079","DOIUrl":"https://doi.org/10.30654/mjcr.10079","url":null,"abstract":"Retinal vasoproliferative tumors are rare, retinal vascular tumours, often diagnosed on routine examination in asymptomatic individuals. In case of symptoms, urgent investigations and treatment is warranted. We report a rare case of a patient suffering from this disease who visited our hospital.","PeriodicalId":92691,"journal":{"name":"Mathews journal of case reports","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69531633","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Aplastic Anemia in Wilson’s disease: A Rare Complication Wilson病再生障碍性贫血：罕见并发症
Mathews journal of case reports Pub Date : 2022-12-15 DOI: 10.30654/mjcr.10078
Aritra Saha, Jinku Ozah, Mriganka Deka, A. Pegu, Somnath Roy, Sofiur Rahman, Yash Duseja
{"title":"Aplastic Anemia in Wilson’s disease: A Rare Complication","authors":"Aritra Saha, Jinku Ozah, Mriganka Deka, A. Pegu, Somnath Roy, Sofiur Rahman, Yash Duseja","doi":"10.30654/mjcr.10078","DOIUrl":"https://doi.org/10.30654/mjcr.10078","url":null,"abstract":"Wilson’s Disease (WD) is an autosomal recessive disease characterized by an excess of copper buildup in the body due to mutations in ATP-7B gene. Wilson’s disease primarily affects liver and basal ganglion of brain, and therefore patients predominantly have hepatic, neuropsychiatric manifestations, which may vary from an asymptomatic state to life threatening fulminant hepatic failure. Diagnosis depends on a high clinical suspicion, typical neurological symptoms, presence of KF ring, decreased serum ceruloplasmin concentration, raised 24 hours urinary copper levels and genetic studies in selected individuals. Pancytopenia due to bone marrow failure is an extremely rare finding in a patient with WD and the exact mechanism for the same is unknown. Here we present the case of a 22-year-old female who presented with features of severe anemia and was eventually diagnosed as a case of WD with bone marrow failure and to the best of our knowledge is a third such case reported worldwide.","PeriodicalId":92691,"journal":{"name":"Mathews journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41467960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Spontaneous Heterotopic Pregnancy: A Case Report and Review of Radiological Assessment and Diagnostic Challenges 自发性异位妊娠：一例病例报告及放射学评估和诊断挑战综述
Mathews journal of case reports Pub Date : 2022-12-07 DOI: 10.30654/mjcr.10076
Biswas Ss
{"title":"Spontaneous Heterotopic Pregnancy: A Case Report and Review of Radiological Assessment and Diagnostic Challenges","authors":"Biswas Ss","doi":"10.30654/mjcr.10076","DOIUrl":"https://doi.org/10.30654/mjcr.10076","url":null,"abstract":"Heterotopic pregnancy is the simultaneous occurrence of intrauterine and extrauterine gestation. It is a rare complication of gestation more common when conception is achieved by assisted reproduction techniques than in natural conceptions. Heterotopic pregnancy is a life-threatening pathology with the diagnosis often missed radiological investigations due to its rarity. A painstaking sonographic evaluation is required to rule out the presence of heterotopic gestation and thus help in prompt diagnosis and appropriate management. Early diagnosis of this pathology reduces the incidence of complications as well as maternal mortality. We hereby report a case of heterotopic pregnancy presenting with gestation amenorrhea of seven weeks and acute pain in the lower abdomen associated with episodes of spotting per vagina of three days duration. The diagnosis of heterotopic pregnancy with ruptured extrauterine gestation was made on a careful ultrasound examination and was managed with exploratory laparotomy. The intrauterine pregnancy course was uneventful with a delivery of a live baby at term. This case report emphasizes the need to carefully examine the adnexa even with the visualization of normal pregnancy on ultrasound interrogation to rule out heterotopic pregnancy.","PeriodicalId":92691,"journal":{"name":"Mathews journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48898824","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Discharging Sinus as a Delayed Complication of Hemithyroidectomy: A Rare Case Report 排血窦作为甲状腺切除术的延迟并发症:一个罕见的病例报告
Mathews journal of case reports Pub Date : 2022-10-19 DOI: 10.30654/mjcr.10075
Grace Budhiraja, Navjot Kaur, Harsimrat Singh
{"title":"Discharging Sinus as a Delayed Complication of Hemithyroidectomy: A Rare Case Report","authors":"Grace Budhiraja, Navjot Kaur, Harsimrat Singh","doi":"10.30654/mjcr.10075","DOIUrl":"https://doi.org/10.30654/mjcr.10075","url":null,"abstract":"Thyroidectomy is known to have a few number of complications such as wound infection, haematoma, recurrent laryngeal nerve or superior laryngeal nerve palsy, hypothyroidism, hypocalcemia, hypertrophied scar formation, and these complications are even less in cases of hemithyroidectomy. We report a rare case of discharging skin sinus of the neck following right hemithyroidectomy which was reported after 12 months of surgery as a late complication. Ultrasonography revealed non fluid retaining sinus tract extending from skin in neck and going deep till the thyroid bed, towards right side at site of right lobe. Excision of sinus tract was done in toto and on incising the specimen, multiple knotted suture materials were found. Histopathology report showed fibrocollagenous stroma with non caseating granuloma with multinucleate giant cell (suture granuloma). The management and review of literature in related to case has been discussed in this case report.","PeriodicalId":92691,"journal":{"name":"Mathews journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45578493","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Spontaneous Thrombosis of a Vein of Galen Malformation in the Adults: Case Report and a Review of the Literature 成人盖伦畸形静脉自发性血栓形成一例报告及文献复习
Mathews journal of case reports Pub Date : 2022-08-05 DOI: 10.30654/mjcr.10074
K. Al Taha, N. Tahhan, C. Dumot, R. Riva, I. Pelissou- Guyotat
{"title":"Spontaneous Thrombosis of a Vein of Galen Malformation in the Adults: Case Report and a Review of the Literature","authors":"K. Al Taha, N. Tahhan, C. Dumot, R. Riva, I. Pelissou- Guyotat","doi":"10.30654/mjcr.10074","DOIUrl":"https://doi.org/10.30654/mjcr.10074","url":null,"abstract":"The vein of Galen malformations (VGAMs) are usually found in childhood and rarely described in adult. There are two major types of presentation: hemodynamic failure in neonates due to massive shunt, and venous hypertension during infancy. VGAMs are treated by endovascular methods in the majority of cases. We present a rare case of a 40 years old patient with incidental finding of VGAM who presented a spontaneous thrombosis and a complete restoration of the deep venous system followed by a review of the literature of resembling cases.","PeriodicalId":92691,"journal":{"name":"Mathews journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46596788","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clioquinol Zinc Ionophore for Terminating Advanced “Decreased Zinc” Testosterone-Dependent Prostate Cancer: A Case Report 氯喹诺锌离子载体终止晚期“低锌”睾酮依赖性前列腺癌1例报告
Mathews journal of case reports Pub Date : 2022-08-03 DOI: 10.30654/mjcr.10073
L. Costello
{"title":"Clioquinol Zinc Ionophore for Terminating Advanced “Decreased Zinc” Testosterone-Dependent Prostate Cancer: A Case Report","authors":"L. Costello","doi":"10.30654/mjcr.10073","DOIUrl":"https://doi.org/10.30654/mjcr.10073","url":null,"abstract":"In 2019, Costello et al. published the first successful treatment Case Report of a patient who presented with testosterone-dependent prostate cancer. That cancer is a “decreased-zinc” malignancy. The treatment was clioquinol zinc ionophore (3% Clioquinol Cream), which terminated the patient’s malignancy. This second Case Report corroborates the 2019 Case report in employing clioquinol to terminate testosterone-dependent prostate cancer in patients. The two patient cases provide evidence that clioquinol will likely be effective for other patients. Now, oncologists and urologists have efficacious systemic chemotherapy for their testosterone-dependent prostate cancer patients. Then, for the first time, many or most of the 314,500 men in the U.S., and the 10 million men worldwide, who die of prostate cancer every year, can now be treated with clioquinol and cured of that cancer. We must make it happen.","PeriodicalId":92691,"journal":{"name":"Mathews journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46650841","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Giant Pedunculated Liver Hemangioma Torsion a Rare Clinical Presentation, Case Report 巨大带蒂肝血管瘤扭转一例罕见临床表现
Mathews journal of case reports Pub Date : 2022-07-18 DOI: 10.30654/mjcr.10072
A. Mohsen, Ansari-Asl Majid
{"title":"Giant Pedunculated Liver Hemangioma Torsion a Rare Clinical Presentation, Case Report","authors":"A. Mohsen, Ansari-Asl Majid","doi":"10.30654/mjcr.10072","DOIUrl":"https://doi.org/10.30654/mjcr.10072","url":null,"abstract":"is is extremely a few occur in lob and more than cases are Our left liver lob originated pedunculated hemangioma which was complicated with torsion. is","PeriodicalId":92691,"journal":{"name":"Mathews journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44361337","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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