Pub Date : 2018-01-01DOI: 10.5336/CASEREP.2017-56165
F. Kurtuluş, Oğuzhan Parlakkiliç, M. T. Yanmaz
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.
{"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}
Pub Date : 2018-01-01DOI: 10.5336/CASEREP.2017-55383
Ö. Solmaz
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
{"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}
Pub Date : 2018-01-01DOI: 10.5336/CASEREP.2017-57351
Pembe Soylu Ustkoyuncu, A. Guven, A. Kiraz, Songul Gokay, Durmuş Doğan
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
{"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}
Pub Date : 2018-01-01DOI: 10.5336/caserep.2017-58826
Tuba Erdem Sultanoğlu, Hasan Sultanoğlu
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,
{"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}
Pub Date : 2018-01-01DOI: 10.5336/CASEREP.2017-58582
D. Turkmen, Kısmet Kaya, O. Sezer
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
{"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}
Pub Date : 2018-01-01DOI: 10.5336/CASEREP.2018-59911
Naoto Shimbori, M. Yayla, A. Yıldız, Duygu Karahacıoğlu, N. Düzgün
who presented with life-threatening multiple thrombosis and who had no signs which met any of the criteria making its diagnosis challenging.
表现出危及生命的多发性血栓形成，没有任何迹象符合任何标准，使其诊断具有挑战性。
{"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}
Pub Date : 2018-01-01DOI: 10.5336/caserep.2017-58089
N. Düzgün, I. Yıldırım
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
{"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}
Pub Date : 2018-01-01DOI: 10.5336/caserep.2018-59805
A. Yorulmaz, Esra Ari, B. Yalçın
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.
{"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}
Pub Date : 2018-01-01DOI: 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}
Pub Date : 2018-01-01DOI: 10.5336/CASEREP.2018-60898
Saime Esin Güney, C. Araz, S. Çehreli
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.
{"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}
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