01341nas a2200217   4500000000100000008004100001260003500042653002100077100001100098700001200109700001200121700001400133700001500147700001200162245008000174856006000254300001000314490000700324520077800331022001401109       2022                            d  bScientific Foundation SPIROSKI10aGeneral Medicine1 aMade M1 aTabri F1 aIlyas F1 aWaspodo N1 aRimayani S1 aKadir D00aA Rare Case of Primary Cutaneous Follicle Center Lymphoma Mimicking Leprosy  uhttps://oamjms.eu/index.php/mjms/article/view/8721/6943  a55-580 v103 a<p>Cutaneous B-Cell Lymphoma is a rare type of cutaneous lymphoma with a plethora of clinical manifestations ranging from macules, papules, nodules, or plaques. The lesions are often painless and certain subtypes such as the primary cutaneous follicle center lymphoma (PCFCL) are indolent. The disease is often misdiagnosed with other dermatoses including bacterial and fungal infections. Here we report a 55-year-old female patient with clinical manifestations resembling multibacillary leprosy that was then confirmed to be PCFCL through aid of dermoscopy and histopathology. The patient then undergone chemotherapy using the R-CHOP regiment which resulted in significant clinical improvement and no signs of metastases or extracutaneous involvement upon follow-up.</p>
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