Results 71 to 80 of about 193,582 (258)

About a rare disease misdiagnosed as malignant lymphoma or tuberculosis: Kikuchi-Fujimoto's disease

open access: yesThe Pan African Medical Journal, 2018
Kikuchi-Fujimoto's disease KFD is a rare and benign cause of cervical lymphadenopathy. It is an anatomoclinical entity of unknown etiology. The confirmation of the diagnosis is always provided by histological lymph node study.
Jawad Lahma   +8 more
doaj   +1 more source

EGFR inhibitor as second-line therapy in a patient with mutant RAS metastatic colorectal cancer: circulating tumor DNA to personalize treatment [PDF]

open access: yes, 2018
A 47-year-old male patient presented in March 2016 to our unit with a palpable painless left supraclavicular mass. A whole-body contrastenhanced computed tomography (CT) scan revealed a left supraclavicular lymphadenopathy, transverse colon thickening ...
Cortesi, Enrico   +3 more
core   +1 more source

The Etiologic Landscape of Lymphoproliferation in Childhood: Proposal for a Diagnostic Approach Exploring from Infections to Inborn Errors of Immunity and Metabolic Diseases

open access: yesTherapeutics and Clinical Risk Management
Giorgio Costagliola,1 Emanuela De Marco,1 Francesco Massei,1 Giulia Roberti,2 Fabrizio Catena,1 Gabriella Casazza,1 Rita Consolini3 1Section of Pediatric Hematology and Oncology, Azienda Ospedaliero-Universitaria Pisana, Pisa, 56126, Italy; 2Pediatrics ...
Costagliola G   +6 more
doaj  

Primary leiomyosarcoma of thyroid with pulmonary metastasis: A diagnostic odyssey

open access: yesClinical Case Reports
Key Clinical Message The presented primary thyroid leiomyosarcoma (TL) case report underscores the importance of recognizing and addressing the diagnostic challenges and management complexities associated with this exceedingly rare malignancy.
Safi Ullah   +6 more
doaj   +1 more source

Griscelli syndrome type 2: A rare and fatal syndrome in a South Indian boy

open access: yesIndian Journal of Pathology and Microbiology, 2016
Griscelli syndrome (GS) is a rare autosomal recessive disorder caused by mutation in the MYO5A (GS1), RAB27A (GS2), and MLPH (GS3) genes, characterized by a common feature, partial albinism.
R Rajyalakshmi, R. N. B. Chakrapani
doaj   +1 more source

Lymphadenopathies: A Retrospective Study of Epidemiology, Characteristics, Diagnosis and Treatment Outcomes of Patients in a Tertiary Hospital in Mogadishu-Somalia

open access: yesInfection and Drug Resistance
Kazım Kıratlı,1 Muhammet Bulut,2 Mukhtar Abdullahi Ali,1 Murat Aysin,3 Ahmed Mohamed Ali,1 Ibrahim Mohamed Hirsi,4 Ahmed Muhammad Bashir5 1Mogadishu Somalia Turkey Recep Tayyip Erdoğan Training and Research Hospital ...
Kıratlı K   +6 more
doaj  

Fever and erythema: exclude all and then… think of Still’s disease!

open access: yesItalian Journal of Medicine, 2016
Adult-onset Still’s disease is a rare disease. Diagnosis of Still’s disease is often difficult to achieve. Herein, we describe our diagnostic approach in a case report regarding an adult patient who presented with fever, erythema, lymphadenopathy and ...
Marta Maset   +5 more
doaj   +1 more source

An unusual unifocal presentation of Castleman’s disease in a young woman with a detailed description of sonographic findings to reduce diagnostic uncertainty: a case report [PDF]

open access: yes, 2013
Background: Castleman’s disease is a rare lymphoproliferative disorder. It typically presents as mediastinal masses and causes a wide range of clinical symptoms.
Maden, Zerrin, Wagner, Norbert
core   +1 more source

The role of mediastinoscopy in the diagnosis of non-lung cancer diseases

open access: yesTherapeutics and Clinical Risk Management, 2017
Serdar Onat,1 Gungor Ates,2 Alper Avcı,3 Tekin Yıldız,4 Ali Birak,1 Cihan Akgul Ozmen,5 Refik Ulku1 1Department of Thoracic Surgery, Faculty of Medicine, Dicle University, 2Department of Chest Diseases, Memorial Hospital, Diyarbakir, 3Department of ...
Onat S   +6 more
doaj  

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