Results 71 to 80 of about 9,394 (232)
JEADV Clinical Practice, EarlyView.ABSTRACT Lupus erythematosus panniculitis (LEP) is a rare variant of cutaneous lupus erythematosus (1%–3% of CLE). There are two case reports to date in the literature of LEP potentially triggered by anti‐TNF‐α therapies. Clinically, it is characterised by tender, erythematous subcutaneous indurated nodules or plaques on fatty body areas.
Cristina Grechin +4 more
wiley +1 more source
Microenvironmental immune cell alterations across the spectrum of nodular lymphocyte predominant Hodgkin lymphoma and T-cell/histiocyte-rich large B-cell lymphoma [PDF]
, 2023 BACKGROUND: The clinicopathological spectrum of nodular lymphocyte predominant Hodgkin lymphoma (NLPHL), also known as nodular lymphocyte predominant B-cell lymphoma, partially overlaps with T-cell/histiocyte-rich large B-cell lymphoma (THRLCBL). NLPHL
Akarca, AU +7 more
core
Lymphoma Classification. [PDF]
, 2020 Twenty-five years after the Revised European American Classification of Lymphoid Neoplasms classification was published, its principle of an integrative approach to disease definition based on several parameters still prevails and has been adopted and ...
de Leval, L., Jaffe, E.S.
core +1 more source
Delayed Treatment Response in a Neonate with Multisystem Langerhans Cell Histiocytosis : Case report and review of literature [PDF]
, 2017 Langerhans cell histiocytosis (LCH) is a rare proliferative disorder of the Langerhans cells, which are part of the mononuclear phagocytic system. The disorder varies in terms of the extent of the disease, its natural course and patient outcomes.
Mandal, Anirban +4 more
core +3 more sources
Granular cell tumor in the pulmonary tree
Respiratory Medicine Case Reports, 2022 Granular cell tumors are often benign growths of the tongue, dermis, and subcutaneous tissues. Rarely, we see production in the pulmonary system. These schwannian and histiocyte origin tumors in the lungs are called pulmonary granulocyte tumors.
Nicholas Nassif +3 more
doaj
Extranodal Rosai-Dorfman disease of the bone treated with surgery and radiotherapy
Rare Tumors, 2014 Rosai-Dorfman disease (RDD) is a rare, benign histiocyte disorder originally described by Rosai and Dorfman in 1969 as sinus histiocytosis with massive lymphadenopathy.
Nitesh N. Paryani +3 more
doaj +1 more source
Plaque‐Like Dermatofibroma: A Case Report and a Review of the Literature With a Focus on Dermoscopy
JEADV Clinical Practice, EarlyView.ABSTRACT Plaque‐like dermatofibroma (PLDF) is a rare clinical variant of dermatofibroma (DF), characterised by flat, infiltrative lesions, often larger than 50 mm in diameter and located on the trunk or lower extremities. A 44‐year‐old male presented to our clinic with a 20 cm brownish plaque with peripheral satellite lesions on the right antecubital ...
Francesco Cavallo +7 more
wiley +1 more source
The 730 nm Picosecond Titanium Sapphire Laser for Treatment of Kratom‐Induced Hyperpigmentation
Lasers in Surgery and Medicine, EarlyView.ABSTRACT Objectives This case series reports the use of the 730‐nm picosecond titanium‐sapphire laser in the treatment of kratom‐induced hyperpigmentation, a dermatological side effect associated with the use of Mitragyna speciosa, which remains poorly understood. Methods A series of patients with kratom‐induced hyperpigmentation were treated using the
Alanoud A. Alhadyani +2 more
wiley +1 more source
Primary histiocytic sarcoma of the central nervous system: A case report
Interdisciplinary Neurosurgery, 2022 Histiocytic sarcoma (HS) is an extremely rare non-Langerhans histiocyte disorder of unknown origin. Recently, biomarkers for the confirmation of HS diagnosis have been reported.
Katsuyuki Negishi +6 more
doaj
Rosai-Dorfman disease with spontaneous resolution: case report of a child
Revista Brasileira de Hematologia e Hemoterapia, 2011 Rosai-Dorfman disease is a self-limiting condition caused by histiocyte proliferation within the sinusoids of lymph nodes and in extranodal tissue. It is a rare disease, particularly in children, that progresses with extensive lymphadenopathy. This paper
Felipe Barbosa Lima +4 more
doaj +1 more source