Results 61 to 70 of about 16,296 (194)
Abstract Background Cancer is the leading cause of death in children aged 1–14 and the second in 15‐19‐year‐old adolescents in Spain. The Paediatric Population‐Based Cancer Registry of the Community of Madrid was created to monitor its incidence and survival.
Raquel López‐González+5 more
wiley +1 more source
Otic Langerhans' Cell Histiocytosis in an Adult: A Case Report and Review of the Literature
Objective. To present a case of otic Langerhans' cell histiocytosis in an adult. Also included the diagnosis and management of the condition and a review of the relevant literature. Case Report.
Anil Gungadeen+2 more
doaj +1 more source
Surveillance of Isolated Colonic Langerhans Cell Histiocytosis in an Adult: A Case Report
Langerhans cell histiocytosis (LCH) is a rare disorder involving the proliferation of myeloid-derived dendritic cells. It most commonly affects children aged less than 1 to 2 years old.
Sandhya Kolagatla MD+3 more
doaj +1 more source
ABSTRACT Background Given the limited research on folate and ferritin status in children with cancer undergoing treatment, we investigated the prevalence of abnormalities and their impact on clinical outcomes and treatment complications. Methods This prospective cohort study enrolled children <18 years diagnosed with cancer between August 2010 and ...
Kalum Withey+5 more
wiley +1 more source
A 37-year-old male case was admitted with goiter. Ultrasonography of thyroid showed a 5 cm cystic nodule in the left lobe with a 1.5 cm solid component. Fine needle aspiration biopsy revealed atypia of undetermined significance or follicular lesion.
A. Bahar Ceyran+5 more
doaj +1 more source
Atypical Presentation of IARS1‐Related Disorder: Expanding the Phenotype and Genotype
ABSTRACT Aminoacyl‐tRNA synthetases (ARSs) catalyze the formation of aminoacyl‐tRNA, which is required for protein translation. A growing number of cases are associated with ARS deficiencies. Pathogenic variants in IARS1 (MIM# 600709), encoding cytoplasmic isoleucyl‐tRNA synthetase, have been associated with autosomal recessive growth retardation ...
Parith Wongkittichote+7 more
wiley +1 more source
Concomitant Langerhans cell histiocytosis of cervical lymph nodes in adult patients with papillary thyroid carcinoma: A report of two cases and review of the literature [PDF]
Objective: Langerhans cell histiocytosis (LCH) is an uncommon entity of unknown etiology. It contains a wide range of clinical presentations. The discovery of oncogenic BRAF V600E mutation in LCH has provided additional evidence that LCH is a neoplasm ...
Al-Ashhab, Maxim+4 more
core +3 more sources
Langerhans cell histiocytosis is an uncommon disease of childhood. Intrathoracic transposition flaps have been described for a management of number of conditions.
Lokavarapu Manoj Joshua+4 more
doaj +1 more source
A Diagnostic Mimic of Lung Cancer: Nodular Pulmonary Amyloidosis Presenting With Cystic Changes
A 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 ...
Supriya Peshin+6 more
wiley +1 more source
Cranial unifocal langerhans cell histiocytosis in a female child: a difficult case with S-100 and CD1a immunonegativity [PDF]
A 13-years old female child was carried to Dr. Sardjito General Hospital, Yogyakarta by her mother with chiefcomplaint of a mass on her forehead. Since eight months prior to her visiting, she had a mass on her forehead whichbecame larger slowly without ...
Soeripto, J Bras, Hanggoro Tri Rinonce Sagiri Mangunsudirdjo
core +1 more source