Scholars Journal of Medical Case Reports最新文献

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Autoimmune Polyendocrinopathy Type 2 (PEA Type) Associated with Biermer's Disease: Report of a Case and Review of the Literature 与比默氏病相关的自身免疫性多内分泌病 2 型(PEA 型):病例报告与文献综述
Scholars Journal of Medical Case Reports Pub Date : 2024-04-08 DOI: 10.36347/sjmcr.2024.v12i04.007
Colna Antonio N´fad, Togo Mamadu, Pr. Yassine Er-Rahali, Pr. Ahmed Anass Guerboub
{"title":"Autoimmune Polyendocrinopathy Type 2 (PEA Type) Associated with Biermer's Disease: Report of a Case and Review of the Literature","authors":"Colna Antonio N´fad, Togo Mamadu, Pr. Yassine Er-Rahali, Pr. Ahmed Anass Guerboub","doi":"10.36347/sjmcr.2024.v12i04.007","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i04.007","url":null,"abstract":"Autoimmune polyendocrinopathy type II (AIEP II) is a more common syndrome that appears mainly in adults. It combines several autoimmune pathologies including Addison's disease and autoimmune thyroid disease (Schmidt syndrome) and/or type 1 diabetes (Carpenter syndrome). We report the case of a 16-year-old patient with notable familial pathological ATCD: Father followed by high blood pressure under antihypertensive treatment and type 2 diabetes under oral anti-diabetes medication. Mother followed for hypothyroidism under hormone replacement treatment with levothyroxine. The patient was followed for hypothyroidism for 2 years, hospitalized in our training for suspicion of adrenal insufficiency. Clinically the patient was asthenic, she had arthralgia and myalgia with anorexia contrasting an appetite for salt with notion of fasting hypoglycemia without melanoderma or vitiligo, the rest of the clinical examination was unremarkable. Weight: 65 kg; Height: 1.69 m; BMI: 23Kg/m²; TT: 70 cm; Pulse: 64 bpm. BP: 110/60 mm Hg in the right arm standing and lying down. Biological exploration found low 08 h plasma cortisol with high ACTH, high TSH and anti-TPO antibodies, and macrocytic normochromic anemia at 8 g/dl with anti-parietal cell antibodies and intrinsic factor have positive. whose explorations were in favor of Biermer's disease. The diagnosis of PEA type 2 was made. The treatment recommended: hormonal replacement of adrenal and thyroid insufficiency as well as vitamin B12 injections with good clinical and biological progress.","PeriodicalId":509943,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140731454","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
Vaginal Angiomyofibroblastoma Associated with Uterine Pathology about a Case 阴道血管肌纤维母细胞瘤伴发子宫病变一例
Scholars Journal of Medical Case Reports Pub Date : 2024-04-05 DOI: 10.36347/sjmcr.2024.v12i04.005
I. Traoré, S. Boudhas, M. Idrissi, N. Mamouni, S. Errarhay, C. Bouchikhi, A. Banani
{"title":"Vaginal Angiomyofibroblastoma Associated with Uterine Pathology about a Case","authors":"I. Traoré, S. Boudhas, M. Idrissi, N. Mamouni, S. Errarhay, C. Bouchikhi, A. Banani","doi":"10.36347/sjmcr.2024.v12i04.005","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i04.005","url":null,"abstract":"Angiomyofibroblastoma is a rare benign mesenchymal tumor. Angiomyofibroblastism is a generally painless tumor, most patients consult for the genes caused the tumor in cases where they are large. We report a case of vaginal location of 3 cm in a 67 years old patient discovered during investigation of abnormal uterine bleeding. The patient benefited complete excision of the tumor, surgical hysteroscopy and hysterectomy by surgical laparoscopy. Angiomyofibroblastoma can be associated with a uterine pathology whose intake in charge cannot be dissociated from it.","PeriodicalId":509943,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140738954","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
Unusual Unveiling: Hodgkin's Lymphoma Manifesting as Chylous Ascites 不寻常的揭幕表现为乳糜腹水的霍奇金淋巴瘤
Scholars Journal of Medical Case Reports Pub Date : 2024-04-05 DOI: 10.36347/sjmcr.2024.v12i04.004
Bounouar Ibtissam, ElManjra Chama, N. Oussama, Lairani Fatima Ezzahra, AitErrami Adil, Oubaha Sophia, Samlani Zouhour, K. Khadija
{"title":"Unusual Unveiling: Hodgkin's Lymphoma Manifesting as Chylous Ascites","authors":"Bounouar Ibtissam, ElManjra Chama, N. Oussama, Lairani Fatima Ezzahra, AitErrami Adil, Oubaha Sophia, Samlani Zouhour, K. Khadija","doi":"10.36347/sjmcr.2024.v12i04.004","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i04.004","url":null,"abstract":"Chylous ascites, an infrequent manifestation of ascites characterized by a triglyceride-rich milky fluid, is associated with lymphatic system disruption resulting from obstruction or post-traumatic injury. It is an unusual complication of lymphomas, which nonetheless represent the primary cause in adults in developed countries, often due to abdominal lymphatic obstruction. We present the case of a 71-year-old woman who presented with abdominal distension attributed to chylous ascites, ultimately revealing non-Hodgkin lymphoma. Palpable peripheral lymph nodes and enlarged lombo-aortic lymph nodes on abdominal CT scans indicated the diagnosis of stage IV centrofollicular non-Hodgkin lymphoma (Ann Arbor classification). The chylous ascites resolved with chemotherapy treatment.","PeriodicalId":509943,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140738551","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 Hydatidosis and Hydatid Pulmonary Embolism 肺水肿病和水肿性肺栓塞
Scholars Journal of Medical Case Reports Pub Date : 2024-04-05 DOI: 10.36347/sjmcr.2024.v12i04.006
Y. Amchich, H. ouzzani, A. Rhorfi, A. Abid
{"title":"Pulmonary Hydatidosis and Hydatid Pulmonary Embolism","authors":"Y. Amchich, H. ouzzani, A. Rhorfi, A. Abid","doi":"10.36347/sjmcr.2024.v12i04.006","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i04.006","url":null,"abstract":"We present an extremely rare case of a old man 52 answith hydatid pulmonary embolism caused by a direct invasion of the pulmonary artery by a hydatid cyst. Even if it is a benign parasitic disease, it can lead to serious complications such as arterial, systemic, or multivisceral dissemination or being responsible for an anaphylactic shock. Because of the clinical polymorphism, the diagnosis can be delayed. Therefore, A chest CT angiography is the gold standard for the positive diagnosis.","PeriodicalId":509943,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140739100","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
Ogilvie Syndrome Induced by Antidepressant: A Case Report 抗抑郁药诱发的奥格尔维综合征:病例报告
Scholars Journal of Medical Case Reports Pub Date : 2024-04-02 DOI: 10.36347/sjmcr.2024.v12i04.003
O. Hadadia, M. Haida, F. Lairani, O. Nacir, A. Errami, S. Oubaha, Z. Samlani, K. Krati
{"title":"Ogilvie Syndrome Induced by Antidepressant: A Case Report","authors":"O. Hadadia, M. Haida, F. Lairani, O. Nacir, A. Errami, S. Oubaha, Z. Samlani, K. Krati","doi":"10.36347/sjmcr.2024.v12i04.003","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i04.003","url":null,"abstract":"Ogilvie’s Syndrome is a rare entity in which the colon becomes massively dilated without apparent mechanical obstruction. Patients on antidepressant drugs commonly complain of dryness of the mouth, tremors, blurring of vision and constipation, which are attributed to the anticholinergic action of the drugs. We report a case of a 39-year-old female case of gastrointestinal complication (pseudo-intestinal obstruction), which are considered rare according to a review of the literature.","PeriodicalId":509943,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140754910","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
Unusual Clinical Synergy: Crohn's Disease, Behçet's Disease, and Ankylosing Spondylodiscitis – A Comprehensive Look at Interactions 不寻常的临床协同作用:克罗恩病、白塞氏病和强直性脊柱盘炎--全面了解相互作用
Scholars Journal of Medical Case Reports Pub Date : 2024-04-01 DOI: 10.36347/sjmcr.2024.v12i04.001
D. Rajih, H. E. Marmouk, F. Lairani, O. Nacir, A. Errami, S. Oubaha, Z. Samlani, K. Krati
{"title":"Unusual Clinical Synergy: Crohn's Disease, Behçet's Disease, and Ankylosing Spondylodiscitis – A Comprehensive Look at Interactions","authors":"D. Rajih, H. E. Marmouk, F. Lairani, O. Nacir, A. Errami, S. Oubaha, Z. Samlani, K. Krati","doi":"10.36347/sjmcr.2024.v12i04.001","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i04.001","url":null,"abstract":"Crohn's disease, Behçet's disease, and ankylosing spondylodiscitis are inflammatory conditions that can pose therapeutic challenges when they occur together. Treatment decisions should be guided by the clinical presentation of each condition, its level of activity, and severity. Several points regarding this combined management need to be addressed. We report the case of a 37-year-old man diagnosed with Crohn's disease, Behçet's disease, and ankylosing spondylodiscitis, aiming to present the diagnostic approach and therapeutic specificities of this association.","PeriodicalId":509943,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140791746","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
Testicular cancer in undescended testicle: A Review of Literature and Case Report 未降睾丸中的睾丸癌:文献综述与病例报告
Scholars Journal of Medical Case Reports Pub Date : 2024-04-01 DOI: 10.36347/sjmcr.2024.v12i04.002
Mehedra Anass, Babty Mouftah, Fouimtizi Jaafar, Slaoui Amine, Karmouni Tarik, E. Khalid, Koutani Abdellatif Iben Attya, Andaloussi Ahmed
{"title":"Testicular cancer in undescended testicle: A Review of Literature and Case Report","authors":"Mehedra Anass, Babty Mouftah, Fouimtizi Jaafar, Slaoui Amine, Karmouni Tarik, E. Khalid, Koutani Abdellatif Iben Attya, Andaloussi Ahmed","doi":"10.36347/sjmcr.2024.v12i04.002","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i04.002","url":null,"abstract":"This clinical case involves a 52-year-old married patient with two children who presented initially with left-sided pelvic pain, leading to the discovery of a tumor on a cryptorchid testicle. Further evaluation revealed a suspicious lesion, indicating degeneration of a testicle in an aberrant position. Surgical intervention via laparoscopic orchidectomy confirmed a seminoma, emphasizing the association between cryptorchidism and testicular germ cell tumors. This case underscores the importance of early diagnosis and management of cryptorchidism to mitigate the risk of testicular malignancies, highlighting the necessity for timely surgical intervention and careful monitoring of patients with undescended testicles.","PeriodicalId":509943,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140774126","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
Deep Neck Infection: A Case Series 颈部深部感染病例系列
Scholars Journal of Medical Case Reports Pub Date : 2024-02-15 DOI: 10.36347/sjmcr.2024.v12i02.013
Ageng Beta Prawatya, Dheo Aliffanandy P. N, Naura Salsabila, Oxa Aqilla Putri S, Ulayya Azzah Nadiroh, Iwan Setiawan Adji
{"title":"Deep Neck Infection: A Case Series","authors":"Ageng Beta Prawatya, Dheo Aliffanandy P. N, Naura Salsabila, Oxa Aqilla Putri S, Ulayya Azzah Nadiroh, Iwan Setiawan Adji","doi":"10.36347/sjmcr.2024.v12i02.013","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i02.013","url":null,"abstract":"Background: Deep neck abscess is a collection of pus (pus) in the potential space between the fascia of the deep neck due to spread from various sources of infection, such as teeth, mouth, throat, paranasal sinuses, ears and neck. Various spaces can be a place for deep neck abscesses including the submandibular, peritonsillar, parapharyngeal, retropharyngeal, submental, parotid, anterior visceral, carotid, and masseter spaces. Inflammation or damage to chronic problem teeth can lead to complications of deep neck abscesses. The main complaint that causes sufferers to come to the hospital is dysphagia, which is difficulty swallowing due to the pain felt by the patient. These complaints can also be accompanied by trismus, stridor caused by tracheal compression, to airway obstruction. Purpose: To determine the progressivity of deep neck abscess so that it can provide medical management until operative incision and drainage. Case report: We report 5 cases of deep neck abscess with management according to the progress of each case. Conclusion: The most common cause or etiology that can lead to deep neck abscess is toothache. Management of deep neck abscess, starting with the administration of empirical antibiotics which is the first step to reduce the infection of bacteria that produce beta lactamase. In deep neck abscess, medical therapy can be given in the form of an antibiotic combination of ceftriaxone with metronidazole, or meropenem with metronidazole as well as surgery in the form of incision and drainage. Treatment can be chosen based on the presence or absence of warning signs and signs of complications. Incision and drainage is performed when complaints do not improve after administration of antibiotics, multiple abscesses and airway obstruction that threatens the patient's life.","PeriodicalId":509943,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139962920","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
Hemorrhagic Hepatic Cyst Mimicking a Cystic Neoplasm: Case Report 模仿囊性肿瘤的出血性肝囊肿:病例报告
Scholars Journal of Medical Case Reports Pub Date : 2024-02-12 DOI: 10.36347/sjmcr.2024.v12i02.012
I. Koti, A. Benhamdane, S. Mrabti, R. Chaibi, S. Hdiye, I. Mouslim, T. Addajou, F. Rouibaa, H. Seddik
{"title":"Hemorrhagic Hepatic Cyst Mimicking a Cystic Neoplasm: Case Report","authors":"I. Koti, A. Benhamdane, S. Mrabti, R. Chaibi, S. Hdiye, I. Mouslim, T. Addajou, F. Rouibaa, H. Seddik","doi":"10.36347/sjmcr.2024.v12i02.012","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i02.012","url":null,"abstract":"Background: Intracystic hemorrhage is an extremely rare complication of simple hepatic cysts. Clinical symptomatology is non-specific, and imaging frequently mimics a biliary cystadenoma or cystadenocarcinoma, which makes it challenging from a diagnostic point of view to an appropriate therapeutic approach. In this report, we present a case of a simple hemorrhagic hepatic cyst mimicking a cystic neoplasm. Case Report: 48-year-old men was referred to our hospital for periumbilical abdominal pain with asthenia and 11 kg weight loss. His physical examination and laboratory findings were unremarkable. Carcinoembryonic antigen concentration was three times higher than normal. Abdominal ultrasonography demonstrated an impure cystic mass measuring 120 x 96 x 108 mm on hepatic segments VI and VII. Abdominal CT showed a cystic mass at the liver possibly related to a cystadenocarcinoma. Abdominal MRI revealed a cystic mass with lobulated contours, located in segments VII, VIII and part of VI, measuring 11.8 x11.4 cm long axis, heterogeneous signal with intense fluid towards the top in T1 and T2 and intense fluid towards the decline in T2 and T1, with the appearance of a small inferior septum slightly enhanced after injection. These findings did not exclude the possibility of malignant cystic tumor, such as biliary cystadenocarcinoma. Therefore, endoscopic ultrasound showed a cystic lesion developing in the liver, with a thickened wall in places, mainly adjacent to an intracystic nodule of 25 mm, this nodule continued with the wall. Biopsy performed using a 22G ultrasound. Aspiration of liquid: string test negative. Pathological examination confirmed a hemorrhagic biliary cyst and there was no tumor tissue. We observed a significant improvement in symptoms and reduction in cyst size after needle aspiration and we decided to adopt a conservative approach. The patient was followed and one year later, the patient remained in good condition without any complaints. ................","PeriodicalId":509943,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139785082","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
Hemorrhagic Hepatic Cyst Mimicking a Cystic Neoplasm: Case Report 模仿囊性肿瘤的出血性肝囊肿:病例报告
Scholars Journal of Medical Case Reports Pub Date : 2024-02-12 DOI: 10.36347/sjmcr.2024.v12i02.012
I. Koti, A. Benhamdane, S. Mrabti, R. Chaibi, S. Hdiye, I. Mouslim, T. Addajou, F. Rouibaa, H. Seddik
{"title":"Hemorrhagic Hepatic Cyst Mimicking a Cystic Neoplasm: Case Report","authors":"I. Koti, A. Benhamdane, S. Mrabti, R. Chaibi, S. Hdiye, I. Mouslim, T. Addajou, F. Rouibaa, H. Seddik","doi":"10.36347/sjmcr.2024.v12i02.012","DOIUrl":"https://doi.org/10.36347/sjmcr.2024.v12i02.012","url":null,"abstract":"Background: Intracystic hemorrhage is an extremely rare complication of simple hepatic cysts. Clinical symptomatology is non-specific, and imaging frequently mimics a biliary cystadenoma or cystadenocarcinoma, which makes it challenging from a diagnostic point of view to an appropriate therapeutic approach. In this report, we present a case of a simple hemorrhagic hepatic cyst mimicking a cystic neoplasm. Case Report: 48-year-old men was referred to our hospital for periumbilical abdominal pain with asthenia and 11 kg weight loss. His physical examination and laboratory findings were unremarkable. Carcinoembryonic antigen concentration was three times higher than normal. Abdominal ultrasonography demonstrated an impure cystic mass measuring 120 x 96 x 108 mm on hepatic segments VI and VII. Abdominal CT showed a cystic mass at the liver possibly related to a cystadenocarcinoma. Abdominal MRI revealed a cystic mass with lobulated contours, located in segments VII, VIII and part of VI, measuring 11.8 x11.4 cm long axis, heterogeneous signal with intense fluid towards the top in T1 and T2 and intense fluid towards the decline in T2 and T1, with the appearance of a small inferior septum slightly enhanced after injection. These findings did not exclude the possibility of malignant cystic tumor, such as biliary cystadenocarcinoma. Therefore, endoscopic ultrasound showed a cystic lesion developing in the liver, with a thickened wall in places, mainly adjacent to an intracystic nodule of 25 mm, this nodule continued with the wall. Biopsy performed using a 22G ultrasound. Aspiration of liquid: string test negative. Pathological examination confirmed a hemorrhagic biliary cyst and there was no tumor tissue. We observed a significant improvement in symptoms and reduction in cyst size after needle aspiration and we decided to adopt a conservative approach. The patient was followed and one year later, the patient remained in good condition without any complaints. ................","PeriodicalId":509943,"journal":{"name":"Scholars Journal of Medical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139844883","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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