Browsing by Author "Oli, Paras"
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Publication Plasma Cell Vulvitis Treated with Platelet-rich Plasma: A Case Report(Nepal Medical Association, 2022) Oli, Paras; Adhikari, Harihar; Thapa, Deeptara PathakAbstract Plasma cell vulvitis is a rare inflammatory disorder of the vulva with an unknown aetiology, characterised by mucosal inflammation. It commonly manifests as pain, itching, dyspareunia, and dysuria and clinically presents as erythematous plaque and macules on the vulva. This condition is refractory to available treatment modalities in the literature. We present a case of a 70-year-old female with histopathologically proven plasma cell vulvitis treated by platelet-rich plasma therapy after multiple failed treatment attempts with topical steroids and immunomodulators. The patient improved both symptomatically and clinically on follow-up with platelet-rich plasma therapy. Platelet-rich plasma which is a new novel treatment can be a therapeutic option for recalcitrant cases of plasma cell vulvitis.Publication Takayasu Arteritis Masquerading as Shoulder Pain: A Case Report(Nepal Medical Association, 2022) Poudel, Prabhat; Oli, Paras; Ojha, Prashant; Yadav, Radhay Shyam; Poudel, Binaya RajAbstract: Takayasu arteritis is a rare progressive chronic granular inflammation of the vessels that mainly affects the aorta and its branches. It is widely distributed in the world population and mainly involves young Asian women, manifesting as a systemic illness with myriads of cardiovascular signs and symptoms. The current case focuses on a young girl who had shoulder pain and weakness as the only manifestation of underlying Takayasu arteritis. Early clinical identification of the disease and control with disease-modifying anti-rheumatic drugs could improve the outcome and prevent devastating sequelae.Publication Takayasu Arteritis Masquerading as Shoulder Pain: A Case Report(Nepal Medical Association, 2022) Poudel, Prabhat; Oli, Paras; Ojha, Prashant; Yadav, Radhay Shyam; Poudel, Binaya RajAbstract Takayasu arteritis is a rare progressive chronic granular inflammation of the vessels that mainly affects the aorta and its branches. It is widely distributed in the world population and mainly involves young Asian women, manifesting as a systemic illness with myriads of cardiovascular signs and symptoms. The current case focuses on a young girl who had shoulder pain and weakness as the only manifestation of underlying Takayasu arteritis. Early clinical identification of the disease and control with disease-modifying anti-rheumatic drugs could improve the outcome and prevent devastating sequelae.