A Diagnostic Mimic of Lung Cancer: Nodular Pulmonary Amyloidosis Presenting With Cystic Changes. [PDF]
Respirol Case RepA 62‐year‐old man with coal workers' pneumoconiosis and a heavy smoking history presented with progressive respiratory symptoms and cystic lung lesions. Surgical biopsy revealed localised AL (kappa) nodular pulmonary amyloidosis, highlighting the need to consider amyloidosis in the differential diagnosis of cystic lung disease with indeterminate ...
Peshin S +6 more
europepmc +2 more sources
Central nervous system crystal-storing histiocytosis: A case report and literature review. [PDF]
Eur J NeurolAbstract Background Crystal‐storing histiocytosis (CSH) is a rare form of histiocytosis with intralysosomal accumulations of immunoglobulins or paraproteins that aggregate as crystals. Central nervous system (CNS) involvement of CSH is uncommon but should be considered in cases of persistent parenchymal enhancement on neuroimaging.
Nathoo N +11 more
europepmc +2 more sources
Solitary pulmonary amyloidoma mimicking lung cancer on 18F-FDG PET-CT scan in systemic lupus erythematosus patient [PDF]
, 2015 Localized amyloid deposits (tumoral amyloidosis or amyloidoma) are uncommon form of amyloidosis and nodular pulmonary amyloidomas are rarely found. This incidental finding can mimic a bronchopulmonary neoplasm and may occur secondarily to an infectious ...
Anić, Branimir +5 more
core +1 more source
Erratum: Indeterminate Cell Histiocytosis: Report of a Case
Acta Medica Iranica, 2015 Alireza Ghanadan +8 more
doaj +1 more source
Hypomorphic mutation in the RAG2 gene affects dendritic cell distribution and migration. [PDF]
, 2013 In Omenn syndrome, altered dendritic cell distribution and impaired migration represent an additional level of immune dysregulation, contributing to the pathogenesis of autoimmunity. OS is a severe combined immunodeficiency characterized by erythrodermia
Anselmo A +10 more
core +1 more source
Multiple brownish macules on child's cheeks. [PDF]
, 2010 n/
Calogero Pagliarello +2 more
core +1 more source
Solitary Type of Congenital Self-healing Reticulohistiocytosis [PDF]
, 2011 Congenital self-healing reticulohistiocytosis is a rare, congenital, benign, self-healing variant of Langerhans cell histiocytosis. It usually appears as multiple papules or nodules; however, occurrence of the solitary type is very rare.
Berger +23 more
core +2 more sources
Integrating multi-disciplinary discussion in clinical practice [PDF]
, 2020 Interstitial lung diseases are very heterogeneous. We present a case of usual interstitial pneumonia pattern on high resolution computed tomography of the chest that was diagnosed successfully after multi-disciplinary discussion. Pulmonologists should be
Afthinos, Andreas +3 more
core +2 more sources
WHO classification of skin tumours: key updates in the fifth edition
Histopathology, EarlyView.This review article summarizes the key updates in the 5th edition of the WHO Classification of Skin Tumours. It provides an overview of the major changes and new entities specific to the skin section, covering areas such as epidermal, melanocytic, mesenchymal and other tumours. The 5th edition of the World Health Organization Classification of Tumours (
Gabrielle Goldman‐Lévy +29 more
wiley +1 more source
Pulmonary langerhans cell histiocytosis [PDF]
, 2012 Pulmonary Langerhans Cell Histiocytosis (PLCH) is a relatively uncommon lung disease that generally, but not invariably, occurs in cigarette smokers. The pathologic hallmark of PLCH is the accumulation of Langerhans and other inflammatory cells in small ...
Nowakowski, Gregorz S +3 more
core +3 more sources