<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Eva Krishna Sutedja</style></author><author><style face="normal" font="default" size="100%">Frizam Dwindamuldan Sutisna</style></author><author><style face="normal" font="default" size="100%">Endang Sutedja</style></author><author><style face="normal" font="default" size="100%">Kartika Ruchiatan</style></author><author><style face="normal" font="default" size="100%">Yogi Faldian</style></author><author><style face="normal" font="default" size="100%">Laila Tsaqilah</style></author><author><style face="normal" font="default" size="100%">Hermin Aminah Usman</style></author><author><style face="normal" font="default" size="100%">Yovan Rivanzah</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Poikilodermatous Mycosis Fungoides: A Rare Case Treated with Low-Dose Methotrexate</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cutaneous T-cell lymphoma</style></keyword><keyword><style  face="normal" font="default" size="100%">Methotrexate</style></keyword><keyword><style  face="normal" font="default" size="100%">Mycosis fungoides</style></keyword><keyword><style  face="normal" font="default" size="100%">Poikilodermatous mycosis fungoides</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">276-279</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Mycosis fungoides (MF) is a subtype of cutaneous T-cell lymphoma (CTCL) and a primary cutaneous lymphoma. Poikilodermatous MF (PMF) is a rare clinical variant of MF. Systemic chemotherapy, such as methotrexate (MTX), may be administered as monotherapy or in combination at low doses in MF. A 64-year-old man with PMF has been reported. History and physical examination revealed hyperpigmented and hypopigmented macules on the chest, abdomen, both arms, back, and upper legs, along with erythematous macules on the right medial thigh. The diagnosis of PMF is based on clinical manifestations and histopathological features of atypical lymphocyte cell infiltration in the epidermis. In addition, immunohistochemical examination also supports the MF diagnosis. The patient received chemotherapy consisting of monotherapy with MTX at low doses. During the third month of observation following MTX therapy, a few of the hyperpigmented and hypopigmented macules appeared to have diminished; some of the erythematous macules had transformed into hyperpigmented macules, and there were no new lesions. The purpose of therapy is to control the disease. Administration of low-dose MTX as a monotherapy may result in clinical improvement, but further observation is necessary. PMF may have a better prognosis than other clinical variants of MF.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Case Report</style></work-type><section><style face="normal" font="default" size="100%">276</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Eva Krishna Sutedja&lt;sup&gt;1&lt;/sup&gt;*, Frizam Dwindamuldan Sutisna&lt;sup&gt;1&lt;/sup&gt;, Endang Sutedja&lt;sup&gt;1&lt;/sup&gt;, Kartika Ruchiatan&lt;sup&gt;1&lt;/sup&gt;, Yogi Faldian&lt;sup&gt;1&lt;/sup&gt;, Laila Tsaqilah&lt;sup&gt;1&lt;/sup&gt;, Hermin Aminah Usman&lt;sup&gt;2&lt;/sup&gt;, Yovan Rivanzah&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Dermatology and Venereology, Faculty of Medicine, Universitas Padjadjaran, Dr. Hasan Sadikin Hospital, Bandung, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Anatomical Pathology, Faculty of Medicine, Universitas Padjadjaran, Dr. Hasan Sadikin Hospital, Bandung, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Eva Krishna Sutedja</style></author><author><style face="normal" font="default" size="100%">Eva Yustiana</style></author><author><style face="normal" font="default" size="100%">Yogi Faldian</style></author><author><style face="normal" font="default" size="100%">Hermin Aminah Usman</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">An Ulcerative Cutaneous Plasmacytosis of the Scalp</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cutaneous plasmacytosis</style></keyword><keyword><style  face="normal" font="default" size="100%">Hypergammaglobulinemia</style></keyword><keyword><style  face="normal" font="default" size="100%">Plasma cell</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">378-381</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Cutaneous plasmacytosis (CP) is a rare benign disorder characterized by polyclonal proliferation of plasma cells of unknown etiology, with potential for malignant transformation. Clinical manifestations include reddish-brown macules, papules, plaques, or nodules, and, infrequently, ulcerative lesions resembling cutaneous squamous cell carcinoma (SCC) or similar cutaneous neoplasms. &lt;strong&gt;Case: &lt;/strong&gt;Herein we reported a case of ulcerative CP which was initially suspected as SCC in a 77–year–old male. Physical examination revealed an ulcer with well–defined borders, and flat edges, with a granulation tissue base on the scalp which was suggested as SCC. Histopathological features showed infiltration of mature plasma cells in the perivascular area, polyclonal plasma cell population on kappa and lambda chain immunohistochemistry, and hypergammaglobulinemia on protein electrophoresis that supported the diagnosis of CP.&lt;strong&gt; Discussion:&lt;/strong&gt; Cutaneous plasmacytosis requires a comprehensive diagnostic evaluation, which typically includes clinical examination, histopathological analysis, immunohistochemistry, ancillary tests such as protein electrophoresis, and negative results from a diagnostic workup for systemic disease. &lt;strong&gt;Conclusion:&lt;/strong&gt; The complexity of CP manifestations necessitates a rigorous diagnostic approach, enabling the differentiation of this benign condition from malignancies with similar presentations.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">378</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Eva Krishna Sutedja&lt;sup&gt;1,*&lt;/sup&gt;, Eva Yustiana&lt;sup&gt;1&lt;/sup&gt;, Yogi Faldian&lt;sup&gt;1&lt;/sup&gt;, Hermin Aminah Usman&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Dermatology and Venereology, Faculty of Medicine, Universitas Padjadjaran - Dr. Hasan Sadikin Hospital, Bandung, West Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Anatomical Pathology, Faculty of Medicine, Universitas Padjadjaran–Dr. Hasan Sadikin General Hospital, Bandung, West Java, INDONESIA.&lt;/p&gt;
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