Results 51 to 60 of about 24,068 (238)
Human Pathology: Case Reports, 2017 Sea-blue histiocytosis is a rare condition that can be often identified in bone marrow, spleen, liver as well as other organs. It can be frequently detected in bone marrow of patients with myeloproliferative neoplasms as well as non-neoplastic conditions
Kacy A. Krehbiel +3 more
doaj +1 more source
Clinical characteristics and survival of children with Langerhans cell hystiocytosis [PDF]
Srpski Arhiv za Celokupno Lekarstvo, 2008 INTRODUCTION Langerhans cell histiocytosis is a rare disease in children, initial presentation is variable, clinical course, prognosis and survival are mostly unpredictable.
Krstovski Nada +3 more
doaj +1 more source
Precision immunomodulation for pediatric hemophagocytic lymphohistiocytosis in intensive care
Pediatric Investigation, EarlyView.This review presents a bedside framework for recognizing pediatric hemophagocytic lymphohistiocytosis and cytokine storm, stabilizing organ dysfunction, identifying the underlying phenotype, selecting targeted immunomodulation, considering extracorporeal adjuncts, and reassessing response within 24–72 h. ABSTRACT Hemophagocytic lymphohistiocytosis (HLH)
Weerapong Lilitwat, Prakreeti Bhandari
wiley +1 more source
Spontaneous resolution of unifocal Langerhans cell histiocytosis of the skull : potential role of ultrasound in detection and imaging follow-up [PDF]
, 2018 Langerhans cell histiocytosis is a tumor-like condition characterized by idiopathic proliferation of Langerhans cells. The disease may involve the skeleton as well as other organs systems. Bone involvement may be solitary or multifocal.
Verlooy, Joris +6 more
core +1 more source
Progressive ocular histiocytosis in a cat
, 2023 Feline progressive histiocytosis is a rare proliferative disorder manifested by solitary or multiple cutaneous nodules and papules with potential late distant metastasis. This case study presents clinical, diagnostic imaging, and histopathologic findings
Akçasız, Zeynep Nilüfer +5 more
core +1 more source
Cutaneous horn: A rare subtype of juvenile xanthogranuloma
Clinical Case Reports, 2020 Because of variability in the JXG shape and the extensive range of a cutaneous horn differential diagnosis, dermatologists should keep this diagnosis in their mind in the time of encountering with infants or children cases of cutaneous horn.
Fariba Iraji +2 more
doaj +1 more source
Case series: Kikuchi‐Fujimoto disease with diagnostic overlap
Rheumatology &Autoimmunity, EarlyView.Kikuchi‐Fujimoto disease (KFD) is a rare, self‐limiting necrotizing lymphadenitis that poses significant diagnostic challenges due to its overlap with tuberculosis, systemic lupus erythematosus (SLE), and malignancy. We present four cases highlighting distinct diagnostic complexities: KFD mimicking tuberculosis with concomitant latent TB infection and ...
Ecem Kalemoglu +6 more
wiley +1 more source
Uncommon variants of Non-Langerhans Cell Histiocytosis [PDF]
, 2019 Background: Histiocytosis are rare disorders of the mononuclear phagocyte system, characterized by a derangement in differentiation, proliferation or function of monocytes and dendritic cells.
Chiara Moltrasio +9 more
core +2 more sources
Rheumatology &Autoimmunity, EarlyView.Summary of pregnancy management in CTD‐ILD across preconception, antenatal, and postpartum phases, emphasizing risk stratification and multidisciplinary care. 6MWT, 6‐min walk test; CTD‐ILD: connective tissue disease‐interstitial lung disease; DLCO, diffusion capacity of the lung for carbon monoxide; FVC, forced vital capacity; MDT, multidisciplinary ...
Khaled Aldhuaina +3 more
wiley +1 more source
CASES OF DISSEMINATED AND GIANT JUVENILE XANTHOGRANULOMA IN CHILDREN
Педиатрическая фармакология, 2014 Juvenile xanthogranuloma is the most common clinical variant of the class II histiocytosis. This article presents two clinical observationsof papulonodular juvenile xanthogranuloma, specification of epidemiological data, clinical and histological ...
E. I. Pil'gui +5 more
doaj +1 more source