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Cerebral Venous Sinus Thrombosis (CVST) as a Rare Presentation of a Brain Hydatid Cyst: A Case Report 脑静脉窦血栓形成（CVST）是罕见的脑棘球蚴：一例报告
Case Reports in Clinical Practice Pub Date : 2023-09-05 DOI: 10.18502/crcp.v8i2.13559
Maryam Kaeedi, Hosein Kaeidi, Mojtaba Shahbazi, Sanaz Heydari Havadaragh, Hamed Amirifard
{"title":"Cerebral Venous Sinus Thrombosis (CVST) as a Rare Presentation of a Brain Hydatid Cyst: A Case Report","authors":"Maryam Kaeedi, Hosein Kaeidi, Mojtaba Shahbazi, Sanaz Heydari Havadaragh, Hamed Amirifard","doi":"10.18502/crcp.v8i2.13559","DOIUrl":"https://doi.org/10.18502/crcp.v8i2.13559","url":null,"abstract":"Cystic hydatidosis is a rare zoonotic condition caused by the larva of the Echinococcus tapeworm. In this disease, brain involvement is a rare condition, accounting for about 2-3% of all cases with hydatid disease. Focal deficits, symptoms of increased intracranial pressure, seizure and mental state changes are most common presentations of CNS cystic echinococcosis. We present a young woman with resistant headache and transient visual obscurations due to increased intra-cranial pressure caused by Cerebral venous sinus thrombosis (CVST) arising from a Hydatid cyst. To the best of our knowledge, this is the first report of hydatid cyst induced CVST. Our case report highlights the importance of considering CVST as an unavoidable complication of brain’s space occupying lesions and especially infective ones as a differential diagnosis.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49009768","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
Charcot Spine Arthropathy (CSA)- a Rare Case Report Charcot脊柱关节病（CSA）——一例罕见病例报告
Case Reports in Clinical Practice Pub Date : 2023-09-05 DOI: 10.18502/crcp.v8i2.13555
Mahendra Singh, Nandlal Bharwani, Navendu Ranjan, Mahesh Bhati
{"title":"Charcot Spine Arthropathy (CSA)- a Rare Case Report","authors":"Mahendra Singh, Nandlal Bharwani, Navendu Ranjan, Mahesh Bhati","doi":"10.18502/crcp.v8i2.13555","DOIUrl":"https://doi.org/10.18502/crcp.v8i2.13555","url":null,"abstract":"Charcot Spine Arthropathy (CSA) is a form of degenerative disease affecting vertebra of lumbar and thoraco-lumbar region. It is commonly seen after injury to the spinal cord or in patients with traumatic paraplegia. It was first described by Kronig in 1884. Case Report- A 35year old male patient presented to our outpatient clinic with complaint of difficulty in changing his position while sitting, lying down, and sitting on a wheel chair. In 2014, he had sustained injury to his spinal cord with bowel and bladder involvement with ASIA-A grade neurology for which long segment fixation was performed from D7-D10 level and the patient was wheel chair bound after surgery. In the present case scenario, the patient was managed conservatively with bed rest, immobilization and medications for pain relief as stated in the existing literature. Conclusion- CSA is a disease of surgical origin commonly seen in patients with spinal cord injury in the past. Although surgery in the form of circumferential arthrodesis is the treatment of choice in most of cases, it is reserved for cases with instability, as it is associated with complications like infections and hardware failure.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45023915","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
Proptosis due to Isolated Intra-orbital Meningocele-a case Report 孤立性眶内脑膜膨出致眼球突出1例报告
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13100
Mohammad Taher Rajabi, Abbas Mohammadi, S. Besharati
{"title":"Proptosis due to Isolated Intra-orbital Meningocele-a case Report","authors":"Mohammad Taher Rajabi, Abbas Mohammadi, S. Besharati","doi":"10.18502/crcp.v8i1.13100","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13100","url":null,"abstract":"Congenital orbital wall defects are very rare bone abnormalities that can cause protrusion of intracranial contents into the orbit. The protrusion of the meninges, which encompasses cerebrospinal fluid (CSF), result in a condition known as the orbital meningocele, a rare cause of pulsatile proptosis. Here, we present a 4-year-old female with left eye proptosis referred to our clinic. On magnetic resonance imaging (MRI), a cystic structure was present. The patient underwent surgery for cyst removal. CSF leakage was noted during surgery. Computed tomography (CT) scan revealed a bony defect in the sphenoid greater wing and the resulting meningocele. Craniotomy surgery was performed to close and fill the defect","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41565577","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
A Case of Antenatal Diagnosis of Ectopia Cordis with Cardiac Disease 心心异位合并心脏病的产前诊断1例
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13098
F. Rashidighader, M. Khorgami, E. Caruso, Farruggio Silvia, Reza Masihi
{"title":"A Case of Antenatal Diagnosis of Ectopia Cordis with Cardiac Disease","authors":"F. Rashidighader, M. Khorgami, E. Caruso, Farruggio Silvia, Reza Masihi","doi":"10.18502/crcp.v8i1.13098","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13098","url":null,"abstract":"Ectopic cordis is a rare anomaly with incidence of 5.5 to 7.9 per one million. In this anomaly, fetal heart is displayed towards outside of the thoracic cavity partially or completely. We describe a case of antenatal diagnosis of Thoracic Ectopia Cordis (EC) with CongenitalHeartDisease (CHD) without any other extracardiac malformations. The mother was referred to our center at 18 weeks of gestation due to abnormal sonography. Fetal Echocardiographic examination showed isolated thoracic ectopia cordis with Double Outlet Right Ventricle (DORV), large inlet to outlet Ventricular Septal Defect (VSD), malposition of Aorta, Pulmonary Atresia with retrograde flow, narrow Pulmonary Artery (PA) and PA branches. Amniocentesis and sonography revealed no other anomaly or chromosomal derangement. Because the diagnosis of Ectopia cordis may be difficult in the fetal period due to multiple factors, meticulous attention should be paid for true diagnosis.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42629612","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
Kimura Disease: a Case Report in an Unlikely age group 木村病:一个不太可能年龄组的病例报告
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13099
Reena Patel, Aradhita Maheshwari, Vijaykumar Gawali
{"title":"Kimura Disease: a Case Report in an Unlikely age group","authors":"Reena Patel, Aradhita Maheshwari, Vijaykumar Gawali","doi":"10.18502/crcp.v8i1.13099","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13099","url":null,"abstract":"Kimura disease is a rare chronic inflammatory disorder of unknown etiology. The disease is primarily seen in young Asian males and is characterized by painless subcutaneous swelling. It is often accompanied by renal involvement, predominantly manifesting as nephrotic syndrome. We describe a case of Kimura disease in a 69-year-old Indian male, presenting with left postauricular swelling. Clinical and histopathological characteristics are described along with a brief review of the literature","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48994025","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 Transformation of Intramural Myoma into Peduncle During Cesarean Section in a 33-year Woman: A Case Report 一例33岁女性剖宫产时壁内肌瘤自发转化为子宫颈的病例报告
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13096
Zahra Yazdi, Seyed Mohammad Hashem Montazeri
{"title":"Spontaneous Transformation of Intramural Myoma into Peduncle During Cesarean Section in a 33-year Woman: A Case Report","authors":"Zahra Yazdi, Seyed Mohammad Hashem Montazeri","doi":"10.18502/crcp.v8i1.13096","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13096","url":null,"abstract":"We report a 33 years multipara pregnant woman who presented with vaginal bleeding due to intramural myoma and preeclampsia. After cesarean section, the myoma changed to the peduncle type and entered the internal space from the inner thickness of the uterus. This infrequent phenomenon made it easier to operate and remove the myoma within a few hours after the cesarean section. Finally, the mother and baby were discharged from the hospital safely after a few days.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46349271","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
Plasma Therapy for Medication-Related Osteonecrosis of the Jaws- a Case Report 血浆治疗颌骨药物相关性骨坏死1例报告
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13088
M. Sadrabad, E. Saberian
{"title":"Plasma Therapy for Medication-Related Osteonecrosis of the Jaws- a Case Report","authors":"M. Sadrabad, E. Saberian","doi":"10.18502/crcp.v8i1.13088","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13088","url":null,"abstract":"Medication-related osteonecrosis of the jaw (MRONJ) is a side effect of anti-bone resorption medications. Nowadays antiresorptive medications like bisphosphonate and monoclonal antibodies like denosumab that have been prescribed for bone disorders and metastatic cancer are becoming increasingly common. Although these medications are quite efficient at reducing bone resorption, they can develop osteomyelitis and jaw necrosis as a side effect. A 65-year-old woman was referred to the Oral Medicine Department of Semnan University of Medical Sciences with diffuse bilateral mandibular osteonecrosis, with a history of osteopetrosis and under-treatment of bisphosphonate. This complication started after tooth extraction and without any healing 5 years ago. After 3 sessions of plasma therapy, obvious improvement was seen. A proper medical history and a routine oral examination before treating with any invasive dental treatment are necessary to avoid any medication-related osteonecrosis of the jaw or mucosal abnormalities.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45207209","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
Acute esophageal necrosis as a result of taking herbal Medicine 服用草药导致急性食道坏死
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13093
Narjes zarei Jalalabadi, Nasim Khajavirad, S. Parsa, Sahar Karimpour reyhan
{"title":"Acute esophageal necrosis as a result of taking herbal Medicine","authors":"Narjes zarei Jalalabadi, Nasim Khajavirad, S. Parsa, Sahar Karimpour reyhan","doi":"10.18502/crcp.v8i1.13093","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13093","url":null,"abstract":"Nowadays People use herbal medicines to try to maintain or improve their health but sometimes they cause side-effects and Some herbal drug may also interact with medication. We reported a 37 -year-old man who presented to the emergency department with sever watery diarrhea, vomiting, dysphagia, bicytopenia, renal failure and Acute esophageal necrosis, also known as black esophagus which is a rare syndrome characterized by a striking diffuse circumferential black appearance of the esophageal mucosa that universally affects the distal esophagus, 2-days after use of herbal drug named suranjan . Suranjan is a herbal formulation used to treat Rheumatoid arthritis","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44044668","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
Right Lower Extremity Numbness- an Atypical Presentation of Acute Aortic Dissection 右下肢麻木——急性主动脉夹层的非典型表现
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13095
Z. Masoumi, Seyed Mojtaba Alavi, M. Sedaqat, M. Shahidi
{"title":"Right Lower Extremity Numbness- an Atypical Presentation of Acute Aortic Dissection","authors":"Z. Masoumi, Seyed Mojtaba Alavi, M. Sedaqat, M. Shahidi","doi":"10.18502/crcp.v8i1.13095","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13095","url":null,"abstract":"Acute aortic dissection (AAD) is one of the most challenging and emergency conditions in the health care system. It`s associated with high mortality. A 55-yearold person was admitted to the emergency department due to numbness of his right leg. The patient had no complaints of chest pain on arrival. However, echocardiography revealed aortic dissection and computed tomography (CT) scan confirmed the diagnosis. The patient was immediately referred to Rajaei hospital for further specialized procedures. He went into the operating room directly and had a successful operation of aortic dissection repair. Rarely AAD has atypical manifestation and may have unusual clinical presentations. Thus, it could cause a delay in establishment of diagnosis of this emergent condition. The purpose of this report was to introduce a rare initial presentation of an atypical aortic dissection.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45199226","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
Pulmonary Artery Aneurysm Dilemma in pregnancy: a Case Report 妊娠期肺动脉瘤的困境1例报告
Case Reports in Clinical Practice Pub Date : 2023-06-28 DOI: 10.18502/crcp.v8i1.13089
Shadi Zamansaraei, Milad Nazari Sabet, Parvin Bahrami
{"title":"Pulmonary Artery Aneurysm Dilemma in pregnancy: a Case Report","authors":"Shadi Zamansaraei, Milad Nazari Sabet, Parvin Bahrami","doi":"10.18502/crcp.v8i1.13089","DOIUrl":"https://doi.org/10.18502/crcp.v8i1.13089","url":null,"abstract":"Pulmonary Artery Aneurysm (PAA), defined as greater than 40 mm dilation of the main pulmonary artery wall, in female and above 43 mm in males is a rare and fatal defect. Since there is a high risk for rupture, especially in cases of symptomatic or severe dilatation, surgical intervention is suggested. There is no recommendation about therapeutic methods based on the diameter of the pulmonary aneurysm in pregnancy in the guidelines. In this rare and unique report, we described a 26-year-old pregnant woman with previous history of biologic pulmonary valve replacement referred to the joint clinic of heart disease and pregnancy at 15 weeks of pregnancy because transthoracic echocardiography showed an aneurysm of the main pulmonary artery (55mm). Due to pulmonary artery diameter and risk of dissection, we informed her about the risks and recommended therapeutic abortion, but she refused and, fortunately no complication occurred during close observation in pregnancy and few months later. There is no specific recommendation about therapeutic methods based on the diameter of the pulmonary aneurysm in pregnancy in the guidelines, but referring to the aortic aneurysm guidelines recommendation, pregnancy termination when PA diameter > 5.5 cm because of the higher risk of dissection. Other factors should be considered to determine the risk of dissection in pregnancy include; categorized PA aneurysms to high or low intravascular PA pressure, PA diameter growth rate, and causative mechanisms. Thus, if pregnancy occurs, decisions about each patient will vary depending on risk factors","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44829196","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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