Results 31 to 40 of about 1,650 (247)

A Case of Chronic Gouty Arthritis with Atypical Localized Tophi

Türk Osteoporoz Dergisi, 2018
Gout disease is an inflammatory disease triggered by monosodium urate monohydrate crystals that accumulate in tissues due to hyperuricemia, which usually seen in males over 40 years.
Samet Sancar Kaya, Mehmet Okcu
doaj   +1 more source

Nasal gouty tophus: Report a rare case presenting as a nasal hump with nasal obstruction

Biomedical Journal, 2016
Dorsal nasal gouty tophus are rare occurrences with limited documentation. Here we report a male patient who has a history of poorly controlled gouty arthritis.
John Chung-Han Wu, Pang-Yun Chou, Chih-Hao Chen   +2 more
doaj   +1 more source

Unusual presentation of gouty tophus in the liver with subsequent appearance in the same site of HCC: a correlate diagnosis? Case report

World Journal of Surgical Oncology, 2019
Background Although gout is a common disease, the presence of gouty tophi outside joints is rare and in literature, there is to date only one report of hepatic tophaceous nodule.
S. Ministrini, G. Baronio, F. Zorzi, L. Bercich, L. Grazioli, S. Molfino, N. Portolani   +6 more
doaj   +1 more source

Cytodiagnosis of gouty tophus

CytoJournal, 2013
To the Editor, Periarticular nodule can prove to be a challenge to both clinicians and pathologists. It covers inflammatory to neoplastic conditions ranging from rheumatoid nodule, gout, giant cell tumor of tendon sheath, synovial osteochondromatosis to synovial sarcoma.[1] Amongst these, gouty tophus is an important differential.
Walke, Vaishali, Ramraje, Sushma, Jadhao, Vinod   +2 more
openaire   +2 more sources

Autologous platelet-rich gel treatment of chronic nonhealing ulcerated tophaceous gout

Indian Journal of Dermatology, 2020
Ulcers resulting from tophaceous gout are uncommon and very difficult to heal. Here we report a case with chronic refractory tophaceous gout, not responding to conventional treatment modality for several months in a 39-year-old man with a 12-year history
Dawei Chen, Chun Wang, Lina Cui, Xingwu Ran   +3 more
doaj   +1 more source

Post-ACL Reconstruction Graft Failure in Severe Gout Arthritis Patient

International Medical Case Reports Journal, 2021
Andri Maruli Tua Lubis, Adisa Yusuf Reksoprodjo, Mohamad Walid Kuncoro, Nadia Nastassia Ifran Department of Orthopedic & Traumatology Cipto Mangunkusumo Hospital, Faculty of Medicine Universitas Indonesia, Jakarta, IndonesiaCorrespondence: Andri Maruli ...
Lubis AMT, Reksoprodjo AY, Kuncoro MW, Ifran NN   +3 more
doaj  

Xanthoma simulating gouty tophus (case report of atypical cholesterol crystal deposition) [PDF]

Exploration of Musculoskeletal Diseases
The most common clinical manifestation of hyperlipidemia is the formation of xanthomas, which are most often localized subcutaneously, sometimes involving tendons and ligaments, and are usually asymptomatic.
Maxim Sergeevich Eliseev, Yanina Igorevna Kuzmina, Maria Nikolaevna Chikina   +2 more
doaj   +1 more source

Feasibility and Safety of Somato‐Cognitive Coordination Therapy for Cerebellar Ataxia Following Pediatric Brain Tumor Treatment

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Cerebellar ataxia after pediatric brain tumor treatment can cause persistent gait, balance, and speech impairment, yet no established rehabilitation strategy exists. Somato‐cognitive coordination therapy (SCCT) is a virtual reality–guided intervention designed to promote sensorimotor integration through visually constrained reaching
Masanobu Takeuchi, Takashi Matsuzawa, Jun Yamanishi, Masahiro Yoshitomi, Junji Ikeda, Shin‐Ichi Tsujimoto, Yasuteru Yamaguchi, Norio Shiba, Dhroov Pathare, Ayumi Kato, Masahiko Hara   +10 more
wiley   +1 more source

Sustained Therapeutic Efficacy of Intravenous Plasminogen Concentrate in Pediatric Patients With Type 1 Plasminogen Deficiency: An Analysis of Dosing Parameters and Clinical Outcomes

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Type 1 plasminogen deficiency (PLGD‐1) is an ultra‐rare autosomal recessive disorder caused by variants in the PLG gene and affects approximately 1.6 individuals per million. The condition is characterized by decreased plasminogen levels and impaired function, resulting in fibrin‐rich lesions on mucous membranes throughout the body.
Charles Nakar, Karen Thibaudeau, Mary Mathias, Heather McDaniel, Madlen Reschke, Klaus Tenbrock, Joseph M. Parker, Amy Shapiro   +7 more
wiley   +1 more source

Guidelines for Pediatric Radiotherapy Simulation: A Report From the Children's Oncology Group Radiation Oncology Discipline

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Pediatric radiation therapy presents unique challenges compared to adult treatments, including those of immobilization, potential need for sedation, and the critical importance of accurate, reproducible positioning. Additionally, heightened attention to imaging doses is necessary to minimize long‐term toxicity in survivors.
Parham Alaei, Stephen Mihalcik, Sujith Baliga, Young Kwok, Dana Casey, Eric Ehler, Christiane Burton, John C. Breneman, Daphne A. Haas‐Kogan, Suzanne L. Wolden, Arnold C. Paulino, Nadia N. Laack, Natia Esiashvili, Sarah Milgrom, Christine Hill‐Kayser, Thomas J. Fitzgerald, John A. Kalapurakal, Chia‐Ho Hua   +17 more
wiley   +1 more source