Pub Date : 2024-05-17DOI: 10.36347/sjmcr.2024.v12i05.047
Rizvan Ali, Muhammad Umair Anjum
Renal lacerations are infrequent but significant injuries that necessitate immediate and proper treatment to avoid complications including bleeding and renal failure. We report a case of a male patient, aged 15, who experienced a kidney laceration due to forceful abdominal trauma. The patient was successfully treated using a combination of conservative methods and surgery, leading to a successful outcome. This example underscores the significance of prompt identification, suitable imaging studies, and quick action in treating kidney lacerations.
{"title":"Renal Laceration Management: A Case Report","authors":"Rizvan Ali, Muhammad Umair Anjum","doi":"10.36347/sjmcr.2024.v12i05.047","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i05.047","url":null,"abstract":"Renal lacerations are infrequent but significant injuries that necessitate immediate and proper treatment to avoid complications including bleeding and renal failure. We report a case of a male patient, aged 15, who experienced a kidney laceration due to forceful abdominal trauma. The patient was successfully treated using a combination of conservative methods and surgery, leading to a successful outcome. This example underscores the significance of prompt identification, suitable imaging studies, and quick action in treating kidney lacerations.","PeriodicalId":21448,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":"104 23","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141126058","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}
Pub Date : 2024-05-17DOI: 10.36347/sjmcr.2024.v12i05.038
Soufiane Habyebete, Ahmed Ameziane, Ali Akjay, Khalid Lmezguidi, A. Ammani, J. Anzaoui
Intravesical Hem-O-Lock clip (HOLC) migration leading to stone formation after laparoscopic radical prostatectomy is a rare and uncommon complication. We report a case of bladder stone witch developed around hem-o-lock clip 2 years after laparoscopic prostatectomy.
{"title":"Bladder Stone after Intravesical Hem-O-Lock Clip Migration 2 Years Following Laparoscopic Radical Prostatectomy","authors":"Soufiane Habyebete, Ahmed Ameziane, Ali Akjay, Khalid Lmezguidi, A. Ammani, J. Anzaoui","doi":"10.36347/sjmcr.2024.v12i05.038","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i05.038","url":null,"abstract":"Intravesical Hem-O-Lock clip (HOLC) migration leading to stone formation after laparoscopic radical prostatectomy is a rare and uncommon complication. We report a case of bladder stone witch developed around hem-o-lock clip 2 years after laparoscopic prostatectomy.","PeriodicalId":21448,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":"105 19","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141126054","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}
Pub Date : 2024-05-17DOI: 10.36347/sjmcr.2024.v12i05.040
B. Zouita, R. Essofi, C. Ahmanna, D. Basraoui, H. Jalal
Our article reports on two cases of pediatric vaginal yolk sac tumors (YSTs), underscoring the diagnostic challenges posed by their similarities to other vaginal tumors, particularly in differentiating from embryonal rhabdomyosarcoma based on clinical and radiological presentations. Emphasizing the critical role of MRI, histological examination, and alpha-fetoprotein levels in diagnosis, we highlight the complexities of treatment, which has evolved from radical surgeries to more conservative approaches with adjuvant chemotherapy, aiming to preserve future sexual and reproductive functions. Our findings advocate for individualized treatment plans and stress the importance of accurate diagnosis and the potential need for alternative therapeutic strategies in cases of atypical response to treatment.
{"title":"Imaging of Vaginal Yolk Sac Tumor: 2 Case Reports and Literature Review","authors":"B. Zouita, R. Essofi, C. Ahmanna, D. Basraoui, H. Jalal","doi":"10.36347/sjmcr.2024.v12i05.040","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i05.040","url":null,"abstract":"Our article reports on two cases of pediatric vaginal yolk sac tumors (YSTs), underscoring the diagnostic challenges posed by their similarities to other vaginal tumors, particularly in differentiating from embryonal rhabdomyosarcoma based on clinical and radiological presentations. Emphasizing the critical role of MRI, histological examination, and alpha-fetoprotein levels in diagnosis, we highlight the complexities of treatment, which has evolved from radical surgeries to more conservative approaches with adjuvant chemotherapy, aiming to preserve future sexual and reproductive functions. Our findings advocate for individualized treatment plans and stress the importance of accurate diagnosis and the potential need for alternative therapeutic strategies in cases of atypical response to treatment.","PeriodicalId":21448,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":"119 50","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141126391","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}
Pub Date : 2024-05-17DOI: 10.36347/sjmcr.2024.v12i05.044
A. Oumoussa, S. T. Eddine, I. Adali, F. Manoudi
In this case report we present the case of three sisters experiencing shared psychotic disorder (SPD), or folie à trois, characterized by the transmission of delusional beliefs within close familial relationships. The primary patient presented aggressive behaviors and paranoid delusions, leading to hospitalization, while the other two siblings displayed similar beliefs but with less severe symptoms. Treatment involved physical separation and pharmacological intervention, resulting in significant improvement, particularly in the induced siblings. The case underscores the importance of a comprehensive approach to managing SPD, combining pharmacotherapy and psychosocial interventions. Further research is needed to improve understanding and optimize treatment strategies for shared delusions. Documenting and sharing such cases can contribute to improved outcomes for patients and their families.
在本病例报告中，我们介绍了三姐妹共同精神障碍（SPD）或三姐妹妄想症（folie à trois）的病例，其特点是妄想信念在亲密的家庭关系中传播。主要患者有攻击性行为和偏执性妄想，导致住院治疗，而另外两个兄弟姐妹则表现出类似的信念，但症状较轻。治疗包括物理分离和药物干预，结果患者病情明显好转，尤其是诱发妄想症的兄弟姐妹。该病例强调了综合治疗 SPD 的重要性，即结合药物治疗和社会心理干预。需要进一步开展研究，以加深对共同妄想症的理解并优化治疗策略。记录和分享此类病例有助于改善患者及其家庭的治疗效果。
{"title":"Exploring Shared Delusions among Three Sisters in Folie à Trois: A Case Report","authors":"A. Oumoussa, S. T. Eddine, I. Adali, F. Manoudi","doi":"10.36347/sjmcr.2024.v12i05.044","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i05.044","url":null,"abstract":"In this case report we present the case of three sisters experiencing shared psychotic disorder (SPD), or folie à trois, characterized by the transmission of delusional beliefs within close familial relationships. The primary patient presented aggressive behaviors and paranoid delusions, leading to hospitalization, while the other two siblings displayed similar beliefs but with less severe symptoms. Treatment involved physical separation and pharmacological intervention, resulting in significant improvement, particularly in the induced siblings. The case underscores the importance of a comprehensive approach to managing SPD, combining pharmacotherapy and psychosocial interventions. Further research is needed to improve understanding and optimize treatment strategies for shared delusions. Documenting and sharing such cases can contribute to improved outcomes for patients and their families.","PeriodicalId":21448,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":"104 8","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141126069","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}
Pub Date : 2024-05-17DOI: 10.36347/sjmcr.2024.v12i05.037
Soufiane Habyebete, Ahmed Ameziane, Ali Akjay, Khalid Lmezguidi, A. Ammani, J. Anzaoui
Sarcoidosis is a systemic granulomatosis of undetermined etiology characterised by the formation of epithelioid and gigantocellular granulomas without caseous necrosis in the affected organs. Our case has a history of sarcoidosis with left flank pain. CT scan founded a left hydronephrosis secondary to a retroperitoneal mass encasing the lumbar ureter which was shunted by a double j stent. Biopsy of the mass showed fibrous tissue with epithelioid and gigantocellular granuloma without caseous necrosis. Our patient is an extremely rare case report.
{"title":"A Rare Case of Retroperitoneal Sarcoidosis","authors":"Soufiane Habyebete, Ahmed Ameziane, Ali Akjay, Khalid Lmezguidi, A. Ammani, J. Anzaoui","doi":"10.36347/sjmcr.2024.v12i05.037","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i05.037","url":null,"abstract":"Sarcoidosis is a systemic granulomatosis of undetermined etiology characterised by the formation of epithelioid and gigantocellular granulomas without caseous necrosis in the affected organs. Our case has a history of sarcoidosis with left flank pain. CT scan founded a left hydronephrosis secondary to a retroperitoneal mass encasing the lumbar ureter which was shunted by a double j stent. Biopsy of the mass showed fibrous tissue with epithelioid and gigantocellular granuloma without caseous necrosis. Our patient is an extremely rare case report.","PeriodicalId":21448,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":"1 17","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141126882","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}
Pub Date : 2024-05-17DOI: 10.36347/sjmcr.2024.v12i05.046
M. Mahir, N. Mennis, H. Ahmanna, B. Zouita, D. Basraoui, H. Jalal
We present the case of a 7-year-old child with a history of tuberculosis exposure, admitted to the pediatric surgery department due to a chronic swelling of the right elbow persisting for 3 years. Despite being afebrile, the patient experienced unspecified weight loss. Clinical examination revealed a painful fluctuating swelling of the right elbow, limited flexion, and a 12-degree valgus deformity of the ulna. Laboratory tests showed an elevated CRP level indicative of an inflammatory process. Standard radiographs exhibited soft tissue hypertrophy without bone lesions. MRI demonstrated synovial hypertrophy of the right elbow joint with adjacent bone marrow infiltration and deformation of the distal humerus. Biopsy revealed nonspecific chronic synovitis. Surgical removal of the synovial mass was performed, and histopathological examination revealed features suggestive of tuberculosis. Extension studies for tuberculosis were negative. The patient was treated with antituberculous therapy and physiotherapy, leading to the regression of symptoms. This case highlights the diagnostic utility of MRI in detecting synovial hypertrophy and bone marrow infiltration in cases of chronic elbow swelling, especially in the context of tuberculosis exposure.
{"title":"The Tuberculous Synovitis of the Elbow: A Misunderstood Entity","authors":"M. Mahir, N. Mennis, H. Ahmanna, B. Zouita, D. Basraoui, H. Jalal","doi":"10.36347/sjmcr.2024.v12i05.046","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i05.046","url":null,"abstract":"We present the case of a 7-year-old child with a history of tuberculosis exposure, admitted to the pediatric surgery department due to a chronic swelling of the right elbow persisting for 3 years. Despite being afebrile, the patient experienced unspecified weight loss. Clinical examination revealed a painful fluctuating swelling of the right elbow, limited flexion, and a 12-degree valgus deformity of the ulna. Laboratory tests showed an elevated CRP level indicative of an inflammatory process. Standard radiographs exhibited soft tissue hypertrophy without bone lesions. MRI demonstrated synovial hypertrophy of the right elbow joint with adjacent bone marrow infiltration and deformation of the distal humerus. Biopsy revealed nonspecific chronic synovitis. Surgical removal of the synovial mass was performed, and histopathological examination revealed features suggestive of tuberculosis. Extension studies for tuberculosis were negative. The patient was treated with antituberculous therapy and physiotherapy, leading to the regression of symptoms. This case highlights the diagnostic utility of MRI in detecting synovial hypertrophy and bone marrow infiltration in cases of chronic elbow swelling, especially in the context of tuberculosis exposure.","PeriodicalId":21448,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":"122 51","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141126228","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}
Pub Date : 2024-05-17DOI: 10.36347/sjmcr.2024.v12i05.043
S. Outaghyame, J. Bouanani, A. Diani, M. Bouroumane, M. Benzalim, S. Alj
Cystic lymphangioma is a congenital anomaly typically detected in early childhood. It predominantly affects the cervical region but can also manifest in other areas such as the mesentery, omentum, and retroperitoneum. Complications, influenced by the lesion's location and size, underscore the critical need for early diagnosis to prevent potential abdominal complications like mesenteric ischemia, volvulus, and bowel obstruction. While radiological imaging may raise suspicion, histological examination remains the definitive diagnostic approach. Treatment primarily involves surgical excision. Here, we present a case of an intra- and retroperitoneal cystic lesion with fatty content on CT and MRI, initially suggestive of either a modified cystic lymphangioma or a teratoma. Subsequent histopathological analysis confirmed the diagnosis of cystic lymphangioma.
{"title":"A Case of Atypical Cystic Lymphangioma with Fatty Content","authors":"S. Outaghyame, J. Bouanani, A. Diani, M. Bouroumane, M. Benzalim, S. Alj","doi":"10.36347/sjmcr.2024.v12i05.043","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i05.043","url":null,"abstract":"Cystic lymphangioma is a congenital anomaly typically detected in early childhood. It predominantly affects the cervical region but can also manifest in other areas such as the mesentery, omentum, and retroperitoneum. Complications, influenced by the lesion's location and size, underscore the critical need for early diagnosis to prevent potential abdominal complications like mesenteric ischemia, volvulus, and bowel obstruction. While radiological imaging may raise suspicion, histological examination remains the definitive diagnostic approach. Treatment primarily involves surgical excision. Here, we present a case of an intra- and retroperitoneal cystic lesion with fatty content on CT and MRI, initially suggestive of either a modified cystic lymphangioma or a teratoma. Subsequent histopathological analysis confirmed the diagnosis of cystic lymphangioma.","PeriodicalId":21448,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":"104 16","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141126063","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}
Pub Date : 2024-05-17DOI: 10.36347/sjmcr.2024.v12i05.048
A. Afif, N. Aballa, S. E. Moussaoui, W. Lahmini, E.E. Kamili, M. Bourrous
The hydatid cyst, or hydatidosis, is a zoonotic infectious disease caused by the development of the larval form of the Echinococcus granulosus tapeworm in humans after accidental ingestion of embryonated eggs, which hatch into oncospheres and transform into hydatid cysts. Renal hydatid cyst is extremely rare in children. The positive diagnosis relies on epidemiological, clinical, radiological, and biological arguments. The standard treatment remains surgery. We report the case of a 5-year-old male child hospitalized for an isolated renal hydatid cyst fistulized into the urinary tract, revealed by lumbalgia and hydatiduria with a proteus mirabilis urinary infection on the cytobacteriological examination of urine. Paraclinical examinations, including ultrasound and uro-CT -scan, aided in diagnosis. Histopathological analysis confirmed the diagnosis of renal hydatidosis. Management was conservative surgical, with partial pericystectomy performed in our patient, resulting in a favorable outcome.
{"title":"Renal Hydatid Cyst in Children: A Case Report","authors":"A. Afif, N. Aballa, S. E. Moussaoui, W. Lahmini, E.E. Kamili, M. Bourrous","doi":"10.36347/sjmcr.2024.v12i05.048","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i05.048","url":null,"abstract":"The hydatid cyst, or hydatidosis, is a zoonotic infectious disease caused by the development of the larval form of the Echinococcus granulosus tapeworm in humans after accidental ingestion of embryonated eggs, which hatch into oncospheres and transform into hydatid cysts. Renal hydatid cyst is extremely rare in children. The positive diagnosis relies on epidemiological, clinical, radiological, and biological arguments. The standard treatment remains surgery. We report the case of a 5-year-old male child hospitalized for an isolated renal hydatid cyst fistulized into the urinary tract, revealed by lumbalgia and hydatiduria with a proteus mirabilis urinary infection on the cytobacteriological examination of urine. Paraclinical examinations, including ultrasound and uro-CT -scan, aided in diagnosis. Histopathological analysis confirmed the diagnosis of renal hydatidosis. Management was conservative surgical, with partial pericystectomy performed in our patient, resulting in a favorable outcome.","PeriodicalId":21448,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":"106 28","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141126023","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}
Pub Date : 2024-05-17DOI: 10.36347/sjmcr.2024.v12i05.049
Mkheittirate Yaacoub, Arioua Abdelilah, Afellah Mohamed, O. Abdelatif, N. Ouattassi, Mohamed Ridal, N. Benmansour, Hammas Nawal, Mohammed Noureddine EL Alami El Amine
Tumors of salivary glands are less frequent in the head and neck region. Pleomorphic adenoma (PA) is a benign tumor of major and accessory salivary glands. The soft palate is one of the most frequent sites among accessory salivary glands. This tumor can increase in size and cause oropharyngeal obstruction with a risk of asphyxia, endangering the patient's life. Treatment is based on complete tumor excision and it’s sometimes difficult. Histopathological examination confirms the diagnosis. In this study, we present a case of a large pleomorphic adenoma of the accessory salivary glands located in the soft palate, successfully treated with intraoral excision surgery after an initial tracheostomy.
{"title":"Soft Palate Pleomorphic Adenoma of a Minor Salivary Gland: An Unusual Presentation","authors":"Mkheittirate Yaacoub, Arioua Abdelilah, Afellah Mohamed, O. Abdelatif, N. Ouattassi, Mohamed Ridal, N. Benmansour, Hammas Nawal, Mohammed Noureddine EL Alami El Amine","doi":"10.36347/sjmcr.2024.v12i05.049","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i05.049","url":null,"abstract":"Tumors of salivary glands are less frequent in the head and neck region. Pleomorphic adenoma (PA) is a benign tumor of major and accessory salivary glands. The soft palate is one of the most frequent sites among accessory salivary glands. This tumor can increase in size and cause oropharyngeal obstruction with a risk of asphyxia, endangering the patient's life. Treatment is based on complete tumor excision and it’s sometimes difficult. Histopathological examination confirms the diagnosis. In this study, we present a case of a large pleomorphic adenoma of the accessory salivary glands located in the soft palate, successfully treated with intraoral excision surgery after an initial tracheostomy.","PeriodicalId":21448,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":"118 23","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141126564","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}
Pub Date : 2024-05-17DOI: 10.36347/sjmcr.2024.v12i05.041
M. A. Lkousse
Chilaiditi sign is a rare phenomenon characterized by the radiological observation of segmental interposition of the colon or small intestine between the liver and the diaphragm. It may manifest asymptomatically or be accompanied by a range of clinical symptoms, from mild abdominal pain to acute intestinal obstruction. When symptoms are present, it is termed Chilaiditi syndrome. Typically, management of Chilaiditi syndrome is conservative; however, surgery may be necessary in cases of complications or failure of conservative therapy.
{"title":"Acute Abdominal Pain Revealing Chilaiditi Syndrome","authors":"M. A. Lkousse","doi":"10.36347/sjmcr.2024.v12i05.041","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i05.041","url":null,"abstract":"Chilaiditi sign is a rare phenomenon characterized by the radiological observation of segmental interposition of the colon or small intestine between the liver and the diaphragm. It may manifest asymptomatically or be accompanied by a range of clinical symptoms, from mild abdominal pain to acute intestinal obstruction. When symptoms are present, it is termed Chilaiditi syndrome. Typically, management of Chilaiditi syndrome is conservative; however, surgery may be necessary in cases of complications or failure of conservative therapy.","PeriodicalId":21448,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":"112 27","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141126654","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}
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