Pub Date : 2020-01-01DOI: 10.5336/caserep.2020-74185
G. Dogan, A. Sığırcı
206 Eosinophilic granuloma is a benign bone disease which is local. It is a mild form of Langerhans cell histiocytosis (LCH). Children, adolescents, and young adults are predominantly affected. The most common site of involvement is the skull.1 Although eosinophilic granuloma (EG) can be asymptomatic and incidentally found, it can be seen as tender, growing scalp mass. A mild head trauma history before clinical symptoms is common.
{"title":"A Case of Eosinophilic Granuloma Presenting as Post-traumatic Scalp Hematoma","authors":"G. Dogan, A. Sığırcı","doi":"10.5336/caserep.2020-74185","DOIUrl":"https://doi.org/10.5336/caserep.2020-74185","url":null,"abstract":"206 Eosinophilic granuloma is a benign bone disease which is local. It is a mild form of Langerhans cell histiocytosis (LCH). Children, adolescents, and young adults are predominantly affected. The most common site of involvement is the skull.1 Although eosinophilic granuloma (EG) can be asymptomatic and incidentally found, it can be seen as tender, growing scalp mass. A mild head trauma history before clinical symptoms is common.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"1 1","pages":"206-210"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81532280","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 : 2020-01-01DOI: 10.5336/caserep.2019-72157
H. Vayvada, C. Demirdöver, E. Tuna, Alper Geyik
women aged 40-55.1,2 The overall risk of breast cancer in the occidental female population is 9.6-13.1% and the risk of death is 3.4%.3 Surgery is the main approach for the treatment of breast cancer. There are several types of breast cancer surgeries and today conservative breast surgery (CBS) is taking the place of radical procedures.4 Mainly, CBS could be classified as wide local excision, quadranectomy, and nipple and skin sparing mastectomy (NSSM). Although there is still a lack of long term data up to date studies for the NSSM, locoregional recurrence is evaluated less than 1% per year which is acceptable when compared to radical and modified radical mastectomy.5
{"title":"Desmoid Fibromatosis Mimicking Breast Cancer After Nipple-Sparing Mastectomy","authors":"H. Vayvada, C. Demirdöver, E. Tuna, Alper Geyik","doi":"10.5336/caserep.2019-72157","DOIUrl":"https://doi.org/10.5336/caserep.2019-72157","url":null,"abstract":"women aged 40-55.1,2 The overall risk of breast cancer in the occidental female population is 9.6-13.1% and the risk of death is 3.4%.3 Surgery is the main approach for the treatment of breast cancer. There are several types of breast cancer surgeries and today conservative breast surgery (CBS) is taking the place of radical procedures.4 Mainly, CBS could be classified as wide local excision, quadranectomy, and nipple and skin sparing mastectomy (NSSM). Although there is still a lack of long term data up to date studies for the NSSM, locoregional recurrence is evaluated less than 1% per year which is acceptable when compared to radical and modified radical mastectomy.5","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"16 1","pages":"95-98"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72906187","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 : 2020-01-01DOI: 10.5336/caserep.2020-74932
M. Güven, Mehmet Şimşek, Müslüm Güneş, S. Tekeş
The disorder usually involves both liver and muscle and is termed glycogen storage diseases type IIIa. However, in about 15% of patients, the disease appears to involve only the liver and is classified as type IIIb. Hypoglycemia, hepatomegaly and progressive myopathy are prominent clinical findings. The presence of a wide variety of mutations in the AGL gene causing disease has been described in the literature.2-4 This new mutation we found in the AGL gene has not been yet published. In this case, we aimed to present our case of a 44-year-old Turkish male diagnosed as glycogen storage disease type IIIa, accompanied by this new mutation with hyperglycemia associated with type 2 diabetes mellitus without hypoglycemia. CASE REPORT A 44-year-old male patient was admitted to our clinic with complaints of inability to walk, dry mouth, polydipsia and polyuria. There is no known family history of diabetes mellitus and glycogen storage disease. Physical exam showed hepatomegaly, muscle weakness and atrophy of the distal extremities. The patient’s height was 165 cm and weight 50 kg.When he was 20 years old, he was diagnosed with glycogen storage disease (GSD) by muscle biopsy due to myopathy but at that time the type of the disease was not determined.The patient first noticed muscle weakness of the distal extremities at the age of 20. The symptoms gradually increased, and he could no longer walk without walking stick. In blood tests, glucose: 262 mg/dl, ALT: 74 U/L, AST: 50 U/L creatinine kinase (CK): 898 U/L HBA1c: 10.3% was detected. The laboratory results of the patient are shown in Table 1. Turkiye Klinikleri J Case Rep. 2020;28(3):173-6
{"title":"Glycogen Storage Disease Type IIIa Presenting with Hyperglycemia: A Novel Mutation","authors":"M. Güven, Mehmet Şimşek, Müslüm Güneş, S. Tekeş","doi":"10.5336/caserep.2020-74932","DOIUrl":"https://doi.org/10.5336/caserep.2020-74932","url":null,"abstract":"The disorder usually involves both liver and muscle and is termed glycogen storage diseases type IIIa. However, in about 15% of patients, the disease appears to involve only the liver and is classified as type IIIb. Hypoglycemia, hepatomegaly and progressive myopathy are prominent clinical findings. The presence of a wide variety of mutations in the AGL gene causing disease has been described in the literature.2-4 This new mutation we found in the AGL gene has not been yet published. In this case, we aimed to present our case of a 44-year-old Turkish male diagnosed as glycogen storage disease type IIIa, accompanied by this new mutation with hyperglycemia associated with type 2 diabetes mellitus without hypoglycemia. CASE REPORT A 44-year-old male patient was admitted to our clinic with complaints of inability to walk, dry mouth, polydipsia and polyuria. There is no known family history of diabetes mellitus and glycogen storage disease. Physical exam showed hepatomegaly, muscle weakness and atrophy of the distal extremities. The patient’s height was 165 cm and weight 50 kg.When he was 20 years old, he was diagnosed with glycogen storage disease (GSD) by muscle biopsy due to myopathy but at that time the type of the disease was not determined.The patient first noticed muscle weakness of the distal extremities at the age of 20. The symptoms gradually increased, and he could no longer walk without walking stick. In blood tests, glucose: 262 mg/dl, ALT: 74 U/L, AST: 50 U/L creatinine kinase (CK): 898 U/L HBA1c: 10.3% was detected. The laboratory results of the patient are shown in Table 1. Turkiye Klinikleri J Case Rep. 2020;28(3):173-6","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"10 1","pages":"173-176"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82466516","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 : 2020-01-01DOI: 10.5336/caserep.2019-72383
Damla Soydan Çabuk, E. M. Canger
122 Osteochondroma is known as the most common benign tumor of osteocartilagenous bones. It accounts for 20-50% of all benign tumors and 10-15% of bone tumors.1 It is characterized by a cartilage-coated exophytic growth originating from the cortex of the bone. However, osteochondroma of craniofacial bones is rare due to intramembraneous origin of the most of the craniomaxillofacial bones. This rare entity is often seen in mandibular condyle or coronoid process. Osteochondroma can be seen in any area with endochondral ossification. The etiology still remains unknown and it may occur at any age.
{"title":"Osteochondroma of the Mandible: A Case Report with an Emphasis on Cone Beam Computed Tomography Features","authors":"Damla Soydan Çabuk, E. M. Canger","doi":"10.5336/caserep.2019-72383","DOIUrl":"https://doi.org/10.5336/caserep.2019-72383","url":null,"abstract":"122 Osteochondroma is known as the most common benign tumor of osteocartilagenous bones. It accounts for 20-50% of all benign tumors and 10-15% of bone tumors.1 It is characterized by a cartilage-coated exophytic growth originating from the cortex of the bone. However, osteochondroma of craniofacial bones is rare due to intramembraneous origin of the most of the craniomaxillofacial bones. This rare entity is often seen in mandibular condyle or coronoid process. Osteochondroma can be seen in any area with endochondral ossification. The etiology still remains unknown and it may occur at any age.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"13 1","pages":"122-125"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84689813","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 : 2020-01-01DOI: 10.5336/caserep.2019-70989
E. Topcu, Zihniye Gonca Okumuş, E. Demirkaya, N. Gündüz, H. Çelik
ABS TRACT Epidermoid cyst can been seen in a variety of locations in the body, but it is rarely seen in the vulvar region, especially in those who do not have a history of genital mutilation. We hereby present a case of an epidermal cyst located in the clitoris for more than 10 years without any symptoms but recently suspected of growth by the patient who consulted a gynecologist. Local surgical removal of the mass is the best practice to be known although long-term effects of the reconstructive procedures in this area is yet to be unknown.
{"title":"Epidermal Cyst of the Clitoris Mimicking Cliteromegaly: A Case Report and Review of the Literatüre","authors":"E. Topcu, Zihniye Gonca Okumuş, E. Demirkaya, N. Gündüz, H. Çelik","doi":"10.5336/caserep.2019-70989","DOIUrl":"https://doi.org/10.5336/caserep.2019-70989","url":null,"abstract":"ABS TRACT Epidermoid cyst can been seen in a variety of locations in the body, but it is rarely seen in the vulvar region, especially in those who do not have a history of genital mutilation. We hereby present a case of an epidermal cyst located in the clitoris for more than 10 years without any symptoms but recently suspected of growth by the patient who consulted a gynecologist. Local surgical removal of the mass is the best practice to be known although long-term effects of the reconstructive procedures in this area is yet to be unknown.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"71 1","pages":"13-16"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78719801","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 : 2020-01-01DOI: 10.5336/caserep.2020-75359
G. Bulut
{"title":"Late-Onset Anaphylaxis due to Irbesartan","authors":"G. Bulut","doi":"10.5336/caserep.2020-75359","DOIUrl":"https://doi.org/10.5336/caserep.2020-75359","url":null,"abstract":"","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"18 1","pages":"272-274"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90848274","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 : 2020-01-01DOI: 10.5336/caserep.2019-73096
E. Ata
condition, it occurs more often in patients under anticoagulation therapy. It can mimic any type of acute abdomen, and sometimes the massive hematoma can be life-threatening.1 RSH is usually managed conservatively, but emergency surgery may be needed in cases with large or progressing hematomas with severe symptoms.2 Here we present a case of 55-year-old female presented with acute epigastric pain three weeks after triple cardiac valve surgery. Abdominal ultrasound (US) and computed tomography (CT) revealed large RSH and ongoing bleeding was detected by repeated US. We found out the RSH associated with superficial epigastric artery (SEA) bleeding by doing selective angiography of left internal mammarian artery (LIMA). The patient was treated successfully by embolization of the bleeding artery through LIMA.
{"title":"Embolisation of Epigastric Artery in a Massive Rectus Sheath Hematoma After Cardiac Valvular Surgery","authors":"E. Ata","doi":"10.5336/caserep.2019-73096","DOIUrl":"https://doi.org/10.5336/caserep.2019-73096","url":null,"abstract":"condition, it occurs more often in patients under anticoagulation therapy. It can mimic any type of acute abdomen, and sometimes the massive hematoma can be life-threatening.1 RSH is usually managed conservatively, but emergency surgery may be needed in cases with large or progressing hematomas with severe symptoms.2 Here we present a case of 55-year-old female presented with acute epigastric pain three weeks after triple cardiac valve surgery. Abdominal ultrasound (US) and computed tomography (CT) revealed large RSH and ongoing bleeding was detected by repeated US. We found out the RSH associated with superficial epigastric artery (SEA) bleeding by doing selective angiography of left internal mammarian artery (LIMA). The patient was treated successfully by embolization of the bleeding artery through LIMA.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"13 1","pages":"87-90"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87798478","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 : 2020-01-01DOI: 10.5336/caserep.2020-73305
S. Ural, Dilruba Güngör, Ömer Faruk Gülaştı
dwarfism with short stature, short body and disproportionate development. This rare genetic disease, which is 0.5-1.5 in 10000 live births, is autosomal dominant inheritance and is common in women. Deficiency of endochondral bone formation and normal periostal bone formation disorder are characteristic; patients have bone deformities and systemic anomalies.1 Atlantoaxial dislocation (AAD) may concurrently exist in achondroplastic patients either de novo, following surgery (foramen magnum decompression) or due to odontoid abnormalities (os odontoideum). Anesthetic management of achondroplastic patients with coexisting AAD offers a complex proposition for anesthesiologists in view of the anatomical and physiological constraints and the possible multisystem involvement.2 In this case report, we aimed to present general anesthesia management in the context of the literature in an achondroplasic patient who was operated due to cardiac tamponade developed after pericardial effusion. CASE REPORT
{"title":"Anesthesia Management in an Acondroplasic Patient Developing Cardiac Tamponade Due to Myxedema","authors":"S. Ural, Dilruba Güngör, Ömer Faruk Gülaştı","doi":"10.5336/caserep.2020-73305","DOIUrl":"https://doi.org/10.5336/caserep.2020-73305","url":null,"abstract":"dwarfism with short stature, short body and disproportionate development. This rare genetic disease, which is 0.5-1.5 in 10000 live births, is autosomal dominant inheritance and is common in women. Deficiency of endochondral bone formation and normal periostal bone formation disorder are characteristic; patients have bone deformities and systemic anomalies.1 Atlantoaxial dislocation (AAD) may concurrently exist in achondroplastic patients either de novo, following surgery (foramen magnum decompression) or due to odontoid abnormalities (os odontoideum). Anesthetic management of achondroplastic patients with coexisting AAD offers a complex proposition for anesthesiologists in view of the anatomical and physiological constraints and the possible multisystem involvement.2 In this case report, we aimed to present general anesthesia management in the context of the literature in an achondroplasic patient who was operated due to cardiac tamponade developed after pericardial effusion. CASE REPORT","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"49 1","pages":"165-168"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87838096","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 : 2020-01-01DOI: 10.5336/caserep.2020-74946
V. Soysal, F. Tokat
{"title":"Malignant Schwannoma of Maxillary Sinus: A Case Report and Review of the Literature","authors":"V. Soysal, F. Tokat","doi":"10.5336/caserep.2020-74946","DOIUrl":"https://doi.org/10.5336/caserep.2020-74946","url":null,"abstract":"","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"15 1","pages":"236-239"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77678768","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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