{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T19:26:09Z","timestamp":1787772369950,"version":"build-2784847793"},"reference-count":18,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"5","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2022,9]]},"abstract":"<jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      Botriomycome-like Kaposi disease is a rare clinical and pathological variant of Kaposi disease. Showing features of pyogenic granuloma (PG) and of Kaposi's sarcoma (KS), it was initially named KS-like PG and considered benign.\n                      <jats:sup>[2]<\/jats:sup>\n                      It is now considered a true KS and was renamed PG-like KS due to the clinical course and the presence of human herpes virus-8 DNA.\n                      <jats:sup>[13],[14]<\/jats:sup>\n                      This entity has been mostly described on the lower extremities, but other rare locations such as hand, nasal mucosa, and face have been reported in the literature.\n                      <jats:sup>[1],[3],[4]<\/jats:sup>\n                      The location on the ear in an immune-competent field, like in our patient, is a very rare finding, and very few cases have been reported in the literature.\n                      <jats:sup>[5]<\/jats:sup>\n                    <\/jats:p>\n                  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