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A Huge Pleomorphic Liposarcoma of the Retroperitoneum 腹膜后巨大多形性脂肪肉瘤
Türkiye Klinikleri Journal of Case Reports Pub Date : 2018-01-01 DOI: 10.5336/CASEREP.2017-56165
F. Kurtuluş, Oğuzhan Parlakkiliç, M. T. Yanmaz
{"title":"A Huge Pleomorphic Liposarcoma of the Retroperitoneum","authors":"F. Kurtuluş, Oğuzhan Parlakkiliç, M. T. Yanmaz","doi":"10.5336/CASEREP.2017-56165","DOIUrl":"https://doi.org/10.5336/CASEREP.2017-56165","url":null,"abstract":"common type of soft tissue sarcomas is liposarcomas. It consists of <1% of all malignant tumors in adulthood.1,2 Retroperitoneal liposarcoma (RLS), is a rare, biologically heterogeneous tumor that presents considerable challenges due to its size and deep location.1 85% of RLS are malignant tumors that remain occult for long periods and grow quite large. Their typical symptoms are discomfort, pain or a palpable mass due to large size. These tumors occur most frequently in men, generally in the fifth or sixth decade of life. Magnetic resonance imaging (MRI) provide reliable data about localization of mass and relationship between vascular structures. Although complete surgical resection is mandatory for extending survival, the majority of patients with huge RLS will develop locally recurrent disease following surgery.1-3 So that patients should be followed routinely in every 3 months during first two years .4 Pleomorphic liposarcoma is the rarest subtype and is a high grade tumor. The risk of recurrence and metastatis with liposarcoma increases with higher grade. Herein, we report a case of a 68 year-old man with a 35 cm mass adjacent to kidney with synchronous inguinal 7 cm mass.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"88 1","pages":"51-54"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91214287","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
Papillary Cystadenoma: Unusual Localization 乳头状囊腺瘤:异常定位
Türkiye Klinikleri Journal of Case Reports Pub Date : 2018-01-01 DOI: 10.5336/CASEREP.2017-55383
Ö. Solmaz
{"title":"Papillary Cystadenoma: Unusual Localization","authors":"Ö. Solmaz","doi":"10.5336/CASEREP.2017-55383","DOIUrl":"https://doi.org/10.5336/CASEREP.2017-55383","url":null,"abstract":"45 apillary cystadenoma of the epididymis (PCE) is the second commonest benign neoplasm of this organ following adenomatoid tumor.1 Its is a rare epithelial tumour which is thought to develop within the efferent ductules.2 It was first described in 1956.3 It may occur sporadically or as a manifestation of von Hippel-Lindau disease (VHLD).4 Only 60 histologically documented cases have been reported in the English-language literature since the original report by Sherrick in 1956.5","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"12 1","pages":"45-47"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79491965","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
X-linked Adrenoleukodystrophy Initially Presenting with Severe Deafness x连锁肾上腺脑白质营养不良最初表现为严重耳聋
Türkiye Klinikleri Journal of Case Reports Pub Date : 2018-01-01 DOI: 10.5336/CASEREP.2017-57351
Pembe Soylu Ustkoyuncu, A. Guven, A. Kiraz, Songul Gokay, Durmuş Doğan
{"title":"X-linked Adrenoleukodystrophy Initially Presenting with Severe Deafness","authors":"Pembe Soylu Ustkoyuncu, A. Guven, A. Kiraz, Songul Gokay, Durmuş Doğan","doi":"10.5336/CASEREP.2017-57351","DOIUrl":"https://doi.org/10.5336/CASEREP.2017-57351","url":null,"abstract":"90 -linked adrenoleukodystrophy (ALD) is the most common peroxisomal disorder characterized by progressive demyelination of the central nervous system and adrenal insufficiency. Poor school performance, attention deficit, behavioral changes, severe visual and hearing impairment are major clinical findings. Hypoglycemia and/or episodes of salt loss, skin hyperpigmentation, quadriplegia and cerebral ataxia may also occur.1","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"24 1","pages":"90-93"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78626455","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
An Advanced Achilles Tendon Rupture During Multidrug Use 多药使用导致晚期跟腱断裂
Türkiye Klinikleri Journal of Case Reports Pub Date : 2018-01-01 DOI: 10.5336/caserep.2017-58826
Tuba Erdem Sultanoğlu, Hasan Sultanoğlu
{"title":"An Advanced Achilles Tendon Rupture During Multidrug Use","authors":"Tuba Erdem Sultanoğlu, Hasan Sultanoğlu","doi":"10.5336/caserep.2017-58826","DOIUrl":"https://doi.org/10.5336/caserep.2017-58826","url":null,"abstract":"resenting the conjoined tendons of the gastrocnemius and soleus muscles, achilles tendon is involved in knee flexion, foot plantar flexion and hindfoot inversion.1 Achilles tendon rupture is a common injury in athletes. It often presents with sudden onset of pain associated with a snapping sound in the lower leg. Patients often describe this sensation as having been kicked or shot in the lower leg. The injury is often disabling,","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"20 1","pages":"126-129"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72639741","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
Two Cases with Aquagenic Palmoplantar Keratoderma 水源性掌足底角化病2例
Türkiye Klinikleri Journal of Case Reports Pub Date : 2018-01-01 DOI: 10.5336/CASEREP.2017-58582
D. Turkmen, Kısmet Kaya, O. Sezer
{"title":"Two Cases with Aquagenic Palmoplantar Keratoderma","authors":"D. Turkmen, Kısmet Kaya, O. Sezer","doi":"10.5336/CASEREP.2017-58582","DOIUrl":"https://doi.org/10.5336/CASEREP.2017-58582","url":null,"abstract":"130 quagenic Palmoplantar Keratoderma (APK) is a rare palmoplantar keratoderma which occurs after short-term contact with water. It was first defined by English et al. in 1996 with the name “transient reactive papulotranslucent acrokeratoderma”.1 Later, it has also been named as aquagenic palmoplantar keratoderma, aquagenic syringeal acrokeratoderma, acquired aquagenic keratoderma, hereditary papulotranslucent acrokeratoderma.2-4","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"583 1","pages":"130-133"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76586548","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
A Rare Clinical Presentation of Behçet's Disease with Life-Threatening Extensive Multiple Thrombosis and Recurrent Cardiac Arrest 罕见的behaperet病伴危及生命的广泛多发性血栓形成和复发性心脏骤停的临床表现
Türkiye Klinikleri Journal of Case Reports Pub Date : 2018-01-01 DOI: 10.5336/CASEREP.2018-59911
Naoto Shimbori, M. Yayla, A. Yıldız, Duygu Karahacıoğlu, N. Düzgün
{"title":"A Rare Clinical Presentation of Behçet's Disease with Life-Threatening Extensive Multiple Thrombosis and Recurrent Cardiac Arrest","authors":"Naoto Shimbori, M. Yayla, A. Yıldız, Duygu Karahacıoğlu, N. Düzgün","doi":"10.5336/CASEREP.2018-59911","DOIUrl":"https://doi.org/10.5336/CASEREP.2018-59911","url":null,"abstract":"who presented with life-threatening multiple thrombosis and who had no signs which met any of the criteria making its diagnosis challenging.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"3 1","pages":"161-165"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73517999","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
Adult-Onset Still's Disease: Persistent Pruritic Erythematous Plaques and Papules 成人发病的Still病:持续性瘙痒性红斑斑块和丘疹
Türkiye Klinikleri Journal of Case Reports Pub Date : 2018-01-01 DOI: 10.5336/caserep.2017-58089
N. Düzgün, I. Yıldırım
{"title":"Adult-Onset Still's Disease: Persistent Pruritic Erythematous Plaques and Papules","authors":"N. Düzgün, I. Yıldırım","doi":"10.5336/caserep.2017-58089","DOIUrl":"https://doi.org/10.5336/caserep.2017-58089","url":null,"abstract":"with features similar to the systemic form of juvenile idiopathic arthritis (sJIA) by Bywaters in 1971.1 It is a rare, acute-onset, systemic inflammatory disease with unknown etiology that is responsible for a significant proportion of cases of fever of unknown orgin. Its pathogenesis is unknown, infectious agents as initiators of the disease have implicated but a definitive agent has been revealed.2 Current opinion that increased cytokine production such as IL-1, IL-6, IL-18, TNF-α and IFNγ plays an important pathophysiological role in AOSD.3","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"16 1","pages":"109-112"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75125243","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
Acquired Partial Lipodystrophy with Autoimmune Thyroiditis 获得性部分脂肪营养不良伴自身免疫性甲状腺炎
Türkiye Klinikleri Journal of Case Reports Pub Date : 2018-01-01 DOI: 10.5336/caserep.2018-59805
A. Yorulmaz, Esra Ari, B. Yalçın
{"title":"Acquired Partial Lipodystrophy with Autoimmune Thyroiditis","authors":"A. Yorulmaz, Esra Ari, B. Yalçın","doi":"10.5336/caserep.2018-59805","DOIUrl":"https://doi.org/10.5336/caserep.2018-59805","url":null,"abstract":"156 ipodystrophies are familial or acquired diseases characterized by a paucity or complete absence of adipose tissue. According to fat tissue loss, lipodystrophies have been classified as generalized, partial or localized lipodystrophy.1,2 Acquired partial lipodystrophy is a rare form of lipodystrophy, which is also known as Barraquer-Simons syndrome or cephalothoracic lipodystrophy.3 Acquired partial lipodystrophy is also recognized as having a close association with autoimmune diseases.4-16 Here, we report a very rare case of acquired partial lipodystrophy accompanied by autoimmune thyroiditis. As far as we know, this is the second case report describing an association between acquired partial lipodystrophy with autoimmune thyroiditis.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"19 1","pages":"156-160"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75133270","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
Angular Pregnancy: Letter to the Editor 怀孕角:给编辑的信
Türkiye Klinikleri Journal of Case Reports Pub Date : 2018-01-01 DOI: 10.5336/CASEREP.2018-60472
M. F. Kıncı, I. Alanbay, K. E. Karaşahin
{"title":"Angular Pregnancy: Letter to the Editor","authors":"M. F. Kıncı, I. Alanbay, K. E. Karaşahin","doi":"10.5336/CASEREP.2018-60472","DOIUrl":"https://doi.org/10.5336/CASEREP.2018-60472","url":null,"abstract":"","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"1 1","pages":"227-228"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74844101","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
Dental Treatment of a Child with Mitochondrial Myopathy Under General Anesthesia 全麻下儿童线粒体肌病的牙科治疗
Türkiye Klinikleri Journal of Case Reports Pub Date : 2018-01-01 DOI: 10.5336/CASEREP.2018-60898
Saime Esin Güney, C. Araz, S. Çehreli
{"title":"Dental Treatment of a Child with Mitochondrial Myopathy Under General Anesthesia","authors":"Saime Esin Güney, C. Araz, S. Çehreli","doi":"10.5336/CASEREP.2018-60898","DOIUrl":"https://doi.org/10.5336/CASEREP.2018-60898","url":null,"abstract":"178 itochondrial myopathies (MM) are uncommon disorders caused by structural and functional abnormalities in mitochondria due to inquietation of the mitochondrial chain of respiration or oxidative phosphorylation.1,2 The condition occurs with an incidence of 1 per 4-5000 live births.3 Primary “target” organs are the central nervous system and the liver but the disorder may account for a wider range of neurologic, endocrine disorders as well as cardiac complications.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"18 1","pages":"178-181"},"PeriodicalIF":0.0,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78908657","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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