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Mucocutaneous Manifestations Among HIV-Infected Patients in Madagascar: Cross-Sectional Study

Mucocutaneous Manifestations Among HIV-Infected Patients in Madagascar: Cross-Sectional Study

Regarding neoplastic diseases, 16 patients presented with Kaposi sarcoma (8 men and 8 women), with 6 patients in the age group of 30-39 years (Figure 3). No case of other types of skin tumors was seen. Toxidermia (Figure 4) was observed in 7 patients, 2 of whom were induced by ART and the other 5 were attributed to antituberculosis drugs and trimethoprim-sulfamethoxazole. Exanthematous rash, the most common type of drug eruption, was seen in 6 cases.

Fandresena Arilala Sendrasoa, Volatiana Mercia Falimiarintsoa, Lala Soavina Ramarozatovo, Fahafahantsoa Rapelanoro Rabenja

JMIR Dermatol 2023;6:e47199

Shortening the Time Interval for the Referral of Patients With Soft Tissue Sarcoma to Expert Centers Using Mobile Health: Retrospective Study

Shortening the Time Interval for the Referral of Patients With Soft Tissue Sarcoma to Expert Centers Using Mobile Health: Retrospective Study

Additionally, 15 (25%) cases were grouped as “other histological subtypes” (including extraskeletal Ewing sarcoma, extraskeletal osteosarcoma, gastrointestinal stromal tumor, perivascular epithelioid cell tumor, giant cell tumor, synovial sarcoma, angiosarcoma, and clear-cell sarcoma). The median tumor size was 90 (IQR 10-450) mm; 10 tumors were not palpable.

Simon Nannini, Nicolas Penel, Emmanuelle Bompas, Thibault Willaume, Jean-Emmanuel Kurtz, Justine Gantzer

JMIR Mhealth Uhealth 2022;10(11):e40718

Quality of Life of Patients With Osteosarcoma in the European American Osteosarcoma Study-1 (EURAMOS-1): Development and Implementation of a Questionnaire Substudy

Quality of Life of Patients With Osteosarcoma in the European American Osteosarcoma Study-1 (EURAMOS-1): Development and Implementation of a Questionnaire Substudy

Treatment outcomes for patients diagnosed during adolescence and young adulthood with the most common bone sarcomas, osteosarcoma (OS), and Ewing sarcoma have improved over the past 30 years with the evidence-based introduction of intensive chemotherapy, wide-margin surgery, and, for some, radiation treatment [1-5]. The 5-year survival rate has improved especially for patients aged younger than 25 years [6].

Gabriele Calaminus, Meriel Jenney, Lars Hjorth, Katja Baust, Mark Bernstein, Stefan Bielack, Patricia De Vos, Pancras C W Hogendoorn, Gordana Jovic, Mark Krailo, Kiana Kreitz, Neyssa Marina, Babasola O Popoola, Cristina Sauerland, Sigbjørn Smeland, Carmen Teske, Clara V Schweinitz, Jeremy Whelan, Andreas Wiener, Matthew R Sydes, Rajaram Nagarajan

JMIR Res Protoc 2019;8(9):e14406