Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1016/j.otohns.2009.11.014 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Seromucinous hamartoma with unique clinical and histopathological features: a case report and review of the literature.
J Med Case Rep
November 2024
Department of anatomical Pathology, Hotel Dieu de France Hospital, Saint Joseph University, Alfred Naccache Boulevard, PO Box: 166830, Ashrafieh, Beirut, Lebanon.
Background: We present this case to highlight the importance of considering seromucinous hamartoma in the differential diagnosis of nasal cavity lesions, particularly due to its rarity and potential for being mistaken for more aggressive pathologies. Seromucinous hamartoma, although benign, can exhibit clinical and histological features that overlap with those of malignant tumors, posing a diagnostic challenge. This case is especially noteworthy due to the unusual presentation of sebaceous differentiation within seromucinous hamartoma, a feature not previously documented in the literature.
View Article and Find Full Text PDFSinonasal adenosquamous carcinomas arising in seromucinous hamartoma or respiratory epithelial adenomatoid hamartoma with atypical features: Report of five detailed clinicopathological and molecular characterisation of rare entity.
Histopathology
November 2024
Department of Pathology, Faculty of Medicine in Plzen, Charles University, Plzen, Czech Republic.
Aims: Sinonasal adenosquamous carcinoma (ASC) is a rare tumour classified as a variant of squamous cell carcinoma, exhibiting both squamous and glandular differentiation. ASC has a poorer prognosis compared to sinonasal mucoepidermoid carcinoma (MEC), another uncommon tumour in this region. ASC is believed to originate from metaplastic squamous epithelium, though it may also arise from respiratory epithelium in respiratory epithelial adenomatoid hamartoma (REAH) or seromucinous glands in seromucinous hamartoma (SH).
View Article and Find Full Text PDFLow-Grade Non-intestinal Type Sinonasal Adenocarcinoma: A Case Report.
Cureus
October 2024
Otolaryngology and Head and Neck Surgery, King Faisal Specialist Hospital and Research Center, Riyadh, SAU.
Sinonasal non-intestinal-type adenocarcinomas represent a rare subset of head and neck cancers with distinct pathological and clinical characteristics. Patients usually present with nasal obstruction, epistaxis, and rhinorrhea. The diagnosis is established through histopathological examination.
View Article and Find Full Text PDFSinonasal Hamartomas.
Surg Pathol Clin
December 2024
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; Laboratory Medicine Program, University Health Network, Toronto General Hospital, 200 Elizabeth Street, Toronto, Ontario M5G 2C4, Canada. Electronic address:
Article Synopsis
- - A range of hamartomatous lesions in the sinonasal tract includes REAH, SH, and NCMH, which have distinct characteristics.
- - REAH and SH show similarities in their appearance and can occur alongside other tumors, leading to ongoing discussions about their classification.
- - NCMH targets a specific patient group and has unique molecular factors, while new related sinonasal hamartomas are also being identified.
Expanding the spectrum of low-grade sinonasal adenocarcinoma with biphasic seromucinous differentiation and activating HRAS/AKT1 mutations.
Histopathology
December 2024
Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
Aims: Low-grade non-intestinal-type sinonasal adenocarcinoma (LGSNAC) is a rare heterogeneous and poorly characterised group of tumours, distinct from intestinal- and salivary-type neoplasms. Therefore, further characterisation is needed for clearer biological understanding and classification.
Methods And Results: Clinical, histological and molecular characterisation of four cases of biphasic, low-grade adenocarcinomas of the sinonasal tract was performed.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!