Volume : 6, Issue : 3, March - 2017

Low-Grade Fibromyxoid SarcomaA Case Report and Review of Literature

M . K. Paswan, M . A. Ansari, A. K. Shrivastav

Abstract :

<p>&nbsp;<span style="text-align: justify;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="text-align: justify;">Low-grade</span><span style="text-align: justify;">&nbsp; </span><span style="text-align: justify;">fiomyxoid </span><span style="text-align: justify;">&nbsp;</span><span style="text-align: justify;">sarcoma </span><span style="text-align: justify;">&nbsp;</span><span style="text-align: justify;">(LGFMS) </span><span style="text-align: justify;">&nbsp;</span><span style="text-align: justify;">is </span><span style="text-align: justify;">&nbsp;</span><span style="text-align: justify;">a rare </span><span style="text-align: justify;">&nbsp;</span><span style="text-align: justify;">neoplasm </span><span style="text-align: justify;">&nbsp;</span><span style="text-align: justify;">with </span><span style="text-align: justify;">&nbsp;</span><span style="text-align: justify;">a </span><span style="text-align: justify;">&nbsp;</span><span style="text-align: justify;">tendency</span></p> <p style="text-align:justify;line-height:115%"><o:p></o:p></p> <p style="text-align:justify;line-height:115%">&nbsp;to &nbsp;develop &nbsp;in &nbsp;deep &nbsp;soft &nbsp;tissue of &nbsp;young &nbsp;adults.<sup> </sup><sup><span style="font-family:&quot;Calii&quot;,sans-serif;mso-bidi-font-family:&#10;&quot;Times New Roman&quot;">(1)</span></sup> It &nbsp;is &nbsp;also &nbsp;referred to &nbsp;as &nbsp;&ldquo;Evans <o:p></o:p></p> <p style="text-align:justify;line-height:115%">tumor&rdquo;, &ldquo;<span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">Hyalinizing&nbsp; spindle cell tumor with giant &nbsp;rosettes&rdquo; and &ldquo;Low-grade <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">fiosarcoma &nbsp;with &nbsp;palisaded &nbsp;granuloma like bodies&rdquo;.<sup>(2,3) </sup>&nbsp;LGFMS is considered a <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">diagnostic &nbsp;dilemma </span>&nbsp;<span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">because &nbsp;of &nbsp;its &nbsp;innocuous &nbsp;and &nbsp;varied &nbsp;histological &nbsp;features &nbsp;that <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">can &nbsp;be &nbsp;potentially &nbsp;confused </span>&nbsp;<span style="mso-bidi-font-size:24.0pt;&#10;line-height:115%">with &nbsp;other &nbsp;benign &nbsp;or &nbsp;low-grade &nbsp;fiomyxoid &nbsp;lesions. <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">This &nbsp;report &nbsp;is &nbsp;aimed &nbsp;at &nbsp;reinforcing </span>&nbsp;<span style="mso-bidi-font-size:24.0pt;&#10;line-height:115%">the &nbsp;need to recognize LGFMS as a sarcoma <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">despite &nbsp;its &nbsp;deceptively &nbsp;benign &nbsp;histological </span>&nbsp;<span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">appearance. <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><b>Case Report:</b><span style="mso-bidi-font-size:24.0pt;line-height:115%"><o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">A &nbsp;20-year-old &nbsp;female &nbsp;patient &nbsp;presented &nbsp;to &nbsp;the surgery &nbsp;Out &nbsp;Patient &nbsp;Department <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">with &nbsp;a &nbsp;painless, deeply &nbsp;situated &nbsp;mass &nbsp;in the proximal extremity (right forearm), <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">present &nbsp;for &nbsp;5 &nbsp;years. &nbsp;&nbsp;Patient &nbsp;was &nbsp;referred &nbsp;to &nbsp;the &nbsp;&nbsp;pathology &nbsp;department &nbsp;for <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">Fine &nbsp;Needle &nbsp;Aspiration &nbsp;Cytology &nbsp;(FNAC). FNAC was &nbsp;suggestive &nbsp;of &nbsp;a &nbsp;benign <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">mesenchymal &nbsp;&nbsp;lesion of &nbsp;neural or fioblastic &nbsp;origin. This was followed by excision. <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">Pathological examination of the excised swelling revealed a grossly circumscribed, <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">Unencapsulated &nbsp;tumor &nbsp;measuring &nbsp;8 x5 x3 cms in size. The cut surface varied from <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">being &nbsp;gray &nbsp;white, firm and fious to gelatinous or &nbsp;&nbsp;myxoid. &nbsp;&nbsp;Microscopy &nbsp;revealed <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">cellular &nbsp;areas &nbsp;constituted &nbsp;by &nbsp;bland &nbsp;spindle &nbsp;shaped &nbsp;fioblasts, &nbsp;alternating &nbsp;with less <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">cellular &nbsp;myxoid &nbsp;areas. A typical &nbsp;pattern of &nbsp;intermixed, sweeping &nbsp;bands &nbsp;of &nbsp;fious and <o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">myxoid &nbsp;tissue, focal &nbsp;areas &nbsp;of &nbsp;storiform &nbsp;architecture &nbsp;and &nbsp;concentric &nbsp;&nbsp;perivascular &nbsp;<o:p></o:p></span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">&nbsp;</span></p> <p style="text-align:justify;line-height:115%"><span style="mso-bidi-font-size:&#10;24.0pt;line-height:115%">cuffs of slender &nbsp;spindle &nbsp;cells &nbsp;was &nbsp;seen ( Figure 1 ).&nbsp;</span><span style="mso-bidi-font-size:24.0pt;line-height:115%;mso-fareast-language:EN-US;&#10;mso-no-proof:yes"><o:p></o:p></span></p>

Keywords :


Cite This Article:

M .K. paswan, M .A. Ansari, A. K. shrivastav, Low-Grade Fibromyxoid Sarcoma–A Case Report and Review of Literature, GLOBAL JOURNAL FOR RESEARCH ANALYSIS : Volume-6, Issue-3, March‾2017


Article No. : 1


Number of Downloads : 1


References :