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10.4103/0019-5154.159664 http://scihub22266oqcxt.onion/10.4103/0019-5154.159664 C4601425!4601425!26538705     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Indian+J+Dermatol 2015 ; 60 (5): 509-11 Nephropedia Template TP {{tp|p=26538705|t=2015. Spindle Cell Hemangioendothelioma: Rare Clinical Entity |pdf=|usr=}}{{26538705}} gab.com Text Spindle Cell Hemangioendothelioma: Rare Clinical Entity JO: Indian J Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=26538705 #FOAvip Spindle-cell hemangioendothelioma (SCHE) comprise a rare subset of vascular tumors, and here, we describe such a case and review the clinical presentation, patho-physiology, differential diagnosis of these tumors to promote early identification and discussion guidance. A 25-years-old male patient presented with multiple painful elevated swellings of both left upper and lower extremities for last 15 years without any systemic involvement. After excluding close differential diagnosis by relevant investigations an excisional biopsy was performed. Based on clinical, radiological and histopathological findings, diagnosis of SCHE was made and full thickness excision and skin grafting were performed. The case is reported due to its rarity and adds our knowledge to the existing literature. Twit Text FOAVip Spindle Cell Hemangioendothelioma: Rare Clinical Entity ????Indian J Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=26538705 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26538705 #FOAvip English Wikipedia <ref>{{Cite pmid|26538705}}</ref> Spindle Cell Hemangioendothelioma: Rare Clinical Entity #MMPMID26538705 Das KD; Ghosh K; Kar C; Gharami RC; Chakraborty S; Bhattacharyya A Indian J Dermatol 2015[Sep]; 60 (5): 509-11 PMID26538705show ga Spindle-cell hemangioendothelioma (SCHE) comprise a rare subset of vascular tumors, and here, we describe such a case and review the clinical presentation, patho-physiology, differential diagnosis of these tumors to promote early identification and discussion guidance. A 25-years-old male patient presented with multiple painful elevated swellings of both left upper and lower extremities for last 15 years without any systemic involvement. After excluding close differential diagnosis by relevant investigations an excisional biopsy was performed. Based on clinical, radiological and histopathological findings, diagnosis of SCHE was made and full thickness excision and skin grafting were performed. The case is reported due to its rarity and adds our knowledge to the existing literature. äSpindle Cell Hemangioendothelioma: Rare Clinical Entity (epmc).pdf DeepDyve Pubget Overpricing