Results 151 to 160 of about 1,106,155 (263)
Multifocal primary cutaneous acral CD8<sup>+</sup> T-cell lymphoproliferative disorder: An atypical presentation. [PDF]
Fritts H +3 more
europepmc +1 more source
The WHO Classification of Genetic Tumour Syndromes: Considerations for Genetics
The WHO Classification of Tumours underpins the diagnosis of neoplastic conditions. The new WHO classification of genetic tumour syndromes (GTS) provides international standards for their diagnosis. This diagram highlights the chromosomal distribution of the genes involved in the GTS covered in this classification.
Ian A. Cree +18 more
wiley +1 more source
A Case of Post-Transplantation Lymphoproliferative Disorder Following Kidney Transplantation. [PDF]
Raval PA +3 more
europepmc +1 more source
ABSTRACT Posaconazole is a triazole antifungal agent used for prophylaxis and treatment of invasive fungal diseases. Posaconazole has high inter‐individual variability in dose‐exposure relationship and benefits from therapeutic drug monitoring (TDM). Adult studies report particularly high rates of subtherapeutic exposure among intensive care unit (ICU)
Kathryn Pavia +2 more
wiley +1 more source
Indolent natural killer-cell lymphoproliferative disorder of the gallbladder: a rare case report. [PDF]
Jiang Y, Xie X, Gao Z, Xu W, Wang Y.
europepmc +1 more source
Journal of General and Family Medicine, Volume 27, Issue 5, September 2026.
Ryuichi Minoda Sada +3 more
wiley +1 more source
ABSTRACT Hidradenitis suppurativa (HS) is a chronic inflammatory skin disorder affecting apocrine gland–bearing areas. We report a 38‐year‐old male with a lesion in the left axilla, initially clinically interpreted as HS and resistant to antibiotics.
R. Gervasi +10 more
wiley +1 more source
Hydroa Vacciniforme Lymphoproliferative Disorder With a Truncating KLF2 Variant Presenting as Benign Photodermatoses. [PDF]
Warner-Levy J +3 more
europepmc +1 more source
Unusual Cutaneous and Lymphatic Findings in an Adult Patient
JEADV Clinical Practice, Volume 5, Issue 3, Page 1023-1025, September 2026.
Sarah Preis +4 more
wiley +1 more source
This review highlights changes relevant to pathologists in the updated multidisciplinary classification of interstitial pneumonias. Changes include expansion beyond idiopathic disease, subclassification as interstitial (fibrotic vs non‐fibrotic) and alveolar filling disorders, expansion to include additional patterns (e.g.
Andrew G Nicholson +7 more
wiley +1 more source

