Pembrolizumab as salvage treatment for T‐cell/histiocyte‐rich and Epstein–Barr virus‐positive large B‐cell lymphoma [PDF]
Alberto Schena +7 more
openalex +1 more source
CD5+ T-Cell/Histiocyte-Rich Large B-Cell Lymphoma [PDF]
Chung‐Che Chang +4 more
openalex +1 more source
Silicosis Diagnosed Using Transbronchial Lung Biopsy: The Pivotal Role of Occupational History
ABSTRACT Pulmonary silicosis, a preventable occupational lung disease caused by chronic inhalation of crystalline silica dust in industries like construction, mining, and stone masonry, remains underdiagnosed in TB‐endemic regions due to overlapping clinical and radiological features.
Boon Hau Ng +6 more
wiley +1 more source
Rituximab plus Ifosfamide, Carboplatin and Etoposide for T-Cell/Histiocyte-Rich B-Cell Lymphoma Arising in Nodular Lymphocyte-Predominant Hodgkins Lymphoma [PDF]
Hyungchul Park +7 more
openalex +1 more source
Refractory Periorbital Necrobiotic Xanthogranuloma Treated With Plasma Cell‐Directed Therapy
eJHaem, Volume 7, Issue 1, February 2026.
Aaron Trando +2 more
wiley +1 more source
Factitious Cheilitis: Report of Two Cases
Differential diagnosis of factitious cheilitis. Conditions affecting the upper lip include perioral dermatitis, herpes simplex, allergic contact dermatitis, and syphilis. Disorders involving the lower lip include actinic cheilitis, atopic cheilitis, irritant contact cheilitis, herpes infection, and candidiasis.
Daniel Mauricio Cuestas Rodriguez +5 more
wiley +1 more source
An unusual acute myeloid leukemia associated with hyper IgE: another case of AML‐M5c? [PDF]
Haematologica. 2001 Feb;86(2):216-7. An unusual acute myeloid leukemia associated with hyper IgE: another case of AML-M5c? Lima M, Orfão A, Coutinho J, Ferreira G, Freitas I, Silvestre F, Justiça B.
COUTINHO, J. +6 more
core
Unusual immunophenotype displayed by histiocytes in haemophagocytic lymphohistiocystosis. [PDF]
Troels Herlin +3 more
openalex +1 more source
ALK‐Positive Histiocytosis With Unilateral Breast Involvement: A Case Report
ABSTRACT APH is a rare disorder characterized by the proliferation of ALK‐expressing histiocytes with variable anatomical involvement; however, mammary involvement is exceptionally rare. A 32‐year‐old woman presented with a painless right breast mass. Ultrasound identified a 9 × 8 mm hypoechoic nodule, categorized as BI‐RADS 4A.
Xuechun Liu, Dong Ren, Yanfang Liang
wiley +1 more source

