Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ali, Kaddah"'
Publikováno v:
Journal of Dermatological Treatment, Vol 34, Iss 1 (2023)
Hereditary progressive mucinous histiocytosis (HPMH) is an extremely rare progressive non-Langerhans cell histiocytic disorder presenting with only cutaneous manifestations. Patients typically present with multiple asymptomatic dome-shaped erythemato
Externí odkaz:
https://doaj.org/article/cc88fb93028e49858cb6c475884518f9
Publikováno v:
Clinical Case Reports, Vol 10, Iss 10, Pp n/a-n/a (2022)
Abstract Leukemia cutis is a cutaneous manifestation of leukemia. Herein, we present a rare cutaneous manifestation of leukemia cutis in a patient with myeloid leukemia m5, characterized by hyperpigmented red‐to‐brown patches on face and upper tr
Externí odkaz:
https://doaj.org/article/5aadf2548df443ae95dc7a3a7d33223d
Autor:
Reem Diab, Zahra Asadi Kani, Ali Kaddah, Mohammad Reza Pourani, Fahimeh Abdollahimajd, Hamideh Moravvej
Publikováno v:
Clinical Case Reports, Vol 10, Iss 2, Pp n/a-n/a (2022)
Abstract A 34‐year‐old female patient presented with recurrent bilateral hypopigmented macules on the labia majora. The lesions were treated with topical steroids, which led to mild improvement, but erosive plaques developed after discontinuing t
Externí odkaz:
https://doaj.org/article/3b111a46d912497f8e412459c093c5b3
Publikováno v:
Anti-Cancer Drugs. 33:970-974
There are no published cases about bullous pyoderma gangrenosum induced by leucovorin, fluorouracil and oxaliplatin (FOLFOX) chemotherapy. With the increasing incidence of gastric and colorectal cancers and the increased usage of targeted therapies,
Autor:
Reem Diab, Mohammad Shahidi-Dadras, Azadeh Rakhshan, Ali kaddah, parsa heydari, Fahimeh Abdollahimajd
Colorectal cancer is a fatal disease that is steadily increasing. Herein, we report a 36-year-old male with a seven-month history of colon adenocarcinoma, who presented with a painless, exophytic, bilateral scrotal mass, mimicking lymphangioma in sha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcde98314e9a470c2a4802972c88482f
https://doi.org/10.22541/au.167241443.39634763/v1
https://doi.org/10.22541/au.167241443.39634763/v1
Publikováno v:
Journal of Dermatological Treatment. 34
Hereditary progressive mucinous histiocytosis (HPMH) is an extremely rare progressive non-Langerhans cell histiocytic disorder presenting with only cutaneous manifestations. Patients typically present with multiple asymptomatic dome-shaped erythemato
Publikováno v:
Dermatologic Therapy. 35