Results 101 to 110 of about 24,068 (238)
Histiocytoses represent a group of diverse rare disorders characterized by the abnormal accumulation of cells derived from the mononuclear phagocyte system in various tissues and organs.
Lucian G. Scurtu +5 more
doaj +1 more source
What Is Your Diagnosis? Cutaneous Mass in a Dog
Veterinary Clinical Pathology, EarlyView.
Ester Quilez, Shannon L. Donahoe
wiley +1 more source
F106 Histiocytosis Infiltrate of Disc
More fully developed and chronic histiocytosis infiltrate of right disc with simultaneous infiltration of the hypothalamus with skin lesions on eye lids and chest. Same patient as F1_05, one year later. Anatomy: Optic disc.
William F. Hoyt, MD
core
Pulmonary Langerhans Cell Histiocytosis
Pulmonary Langerhans cell histiocytosis is an uncommon interstitial lung disease that results from the accumulation of cells known as Langerhans cells in the lung. It primarily affects young smokers. High resolution chest computed tomography findings are
Furtun K. +5 more
core +1 more source
The clinicopathological characteristics and differential diagnosis of histiocytosis
The histiocytosis is divided into Langerhans' cell histiocytosis (histiocytosis X) and non-Langerhans' cell histiocytosis (NLCH). The former mainly occurs in lymphatic hematopoietic tissue and often involves central nervous system (CNS).
Shi-zhu YU
doaj
Ventilation Imaging of the Lung at 0.55T With Continuous Slice Cycling
ABSTRACT Purpose To propose and evaluate a novel method for pulmonary ventilation imaging, offering considerably improved SNR. Methods A continuous slice cycling (CSC) acquisition scheme is proposed to exclusively capture signal modulations from respiratory motion with increased SNR.
Andrea Leuthard +4 more
wiley +1 more source
Langerhans’ cell histiocytosis (histiocytosis X): A rare and diverse group of disorder in children [PDF]
Langerhans cell histiocytosis is a rare disorder of unknown etiology with proliferation of Langerhans’ cells which may infiltrate a single or multiple organs.
Prajapati, Snehal +2 more
core
ALK‐Positive Histiocytosis With Unilateral Breast Involvement: A Case Report
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.
Xuechun Liu, Dong Ren, Yanfang Liang
doaj +1 more source
A 50‐year‐old woman presented with recurrent spontaneous pneumothorax and bilateral pulmonary cysts. Whole‐exome sequencing identified a pathogenic FLCN variant, confirming Birt‐Hogg‐Dubé (BHD) syndrome 15 years after symptom onset. This case highlights BHD as an underrecognized cause of diffuse cystic lung disease.
Chia‐Ni Liu +2 more
wiley +1 more source
Cutaneous Langerhans Cell Histiocytosis
We report a 4-year-old boy with localized Langerhans cell histiocytosis. The lesions were restricted to the skin of his back, eyelids, glans penis and prepuce for 2 years. Histopathological and electron microscopic examinations showed typical features of
吳亮遠;蔡呈芳;陳佑甫;洪志明 +1 more
core

