Results 151 to 160 of about 24,104 (312)
ABSTRACT Chest‐wall Ewing sarcoma (CWES) is uncommon in adults and often abuts vital thoracic structures, making R0 resection challenging despite gains with multimodal therapy. A 46‐year‐old Arab male presented with year‐long right‐sided chest pain, weight loss, and a firm mass over the lower right ribs.
Mohammad Alaa Aldakak +5 more
wiley +1 more source
Parotid neoplasms: analysis of 600 patients attended at a single institution [PDF]
Ademar Takahama +2 more
openalex +3 more sources
Delayed Diagnosis of Sézary Syndrome: Lessons From a Psoriasiform Presentation
ABSTRACT Pruritic erythroderma is not always psoriasis. Resistant cases require a broad evaluation for cutaneous lymphoma. Early, timely diagnosis prevents disease progression, improves outcomes, and enhances quality of life, highlighting the need for re‐evaluation when conventional treatments fail.
Sudhan Neupane +3 more
wiley +1 more source
Solitary fibrous tumor of deep parotid gland preoperatively classified as salivary gland neoplasm of uncertain malignant potential by the Milan system for reporting salivary gland cytopathology: A common diagnosis for a rare entity [PDF]
Hamza N. Gokozan, Theresa Scognamiglio
openalex +1 more source
Limbal Mass as a Presentation of Parotid Gland Undifferentiated Carcinoma: A Case Report
Metastatic neoplasms to the ocular surface are extremely rare. Here, we describe a case of A 56-year-old man developed simultaneously a limbal and parotid gland masses in his left side.
Mitra Akbari +2 more
doaj
P291 Three centre experience of extracapsular dissection of benign parotid neoplasms
Mariana P. Monteiro +5 more
openalex +2 more sources
Malignant fibrohistiocytoma of the parotid region : report of a case [PDF]
Most salivary gland tumors are benign, malignant lesions accounting for 15-30% of the total. The most frequent site of salivary gland neoplasms is the parotid gland (80% of all cases).
Alba García, José Ramón +4 more
core
ABSTRACT Background Because salivary gland cancers (SGC) are rare and include different tumor subtypes, data on their long‐term quality of life and late toxicities are sparse. Methods Multi‐national study including SGC survivors more than 5 years after diagnosis.
Susanne Singer +26 more
wiley +1 more source

