Results 71 to 80 of about 23,113 (277)

Assessment of Deep Convolutional Neural Network Models for the Classification of Benign Fibro‐Osseous Lesions of the Jaws

open access: yesClinical and Experimental Dental Research, Volume 11, Issue 6, December 2025.
ABSTRACT Objectives Benign fibro‐osseous lesions (BFOL) constitute a group of pathologic entities with marked overlapping histopathologic features but are diverse in nature and clinical behaviors. Accurate diagnoses of BFOLs necessitate clinical‐pathological correlations, which are paramount for their appropriate management.
Paniti Achararit   +5 more
wiley   +1 more source

Diagnostic Imaging of Primary Cutaneous Osteoma of the Forehead

open access: yesCase Reports in Dermatology
Introduction: Osteoma cutis is a rare benign cutaneous nodule characterized by ectopic bone formation in the dermis or subcutaneous tissue.
Soma Nakaso   +3 more
doaj   +1 more source

SATB2 is Rarely Expressed in Endometrial or Endocervical Carcinoma

open access: yesAPMIS, Volume 133, Issue 12, December 2025.
ABSTRACT Special AT‐rich sequence‐binding protein 2 (SATB2) can distinguish primary ovarian mucinous tumors from ovarian metastases of colorectal or appendiceal tumors. However, its expression in other gynecological localizations remains underexplored.
Tatiana Amaamri‐Seebach   +4 more
wiley   +1 more source

Mastoid osteoma: a case report [PDF]

open access: yes, 2016
Mastoid osteoma is a rare benign neoplasm of mesenchymal origin. Osteomas of the temporal bone are infrequent, and these mastoid osteomas are a definite rare occurrence. These tumours can present with cosmetic deformity and sometimes with pain.
Doi, Mohamad   +2 more
core  

Mouse Models of Osteosarcoma: Unraveling Disease Mechanisms and Accelerating Drug Discovery and Development

open access: yesCancer Reports, Volume 8, Issue 11, November 2025.
ABSTRACT Background Osteosarcoma is the most frequent primary bone malignancy, affecting mainly children, adolescents, and young adults. For the past 40 years, improvements in the survival of patients with osteosarcoma have been minimal, primarily as a consequence of the lack of systemic therapy options beyond traditional cytotoxic agents.
Staci L. Haney, Sarah A. Holstein
wiley   +1 more source

Multiple miliary osteoma cutis treatment response to Q-switched Nd:YAG laser: A case report

open access: yesSAGE Open Medical Case Reports, 2020
Facial multiple miliary osteoma cutis is a variant of osteoma cutis usually occurring in women with a previous history of acne vulgaris. Successful ablative laser treatment has been reported using both CO2 and Er:YAG lasers among other invasive treatment
Augustin C. Barolet   +2 more
doaj   +1 more source

Mucosal Grafts and Flaps in Draf IIb and Draf III: A Systematic Review and Meta‐analysis

open access: yesOtolaryngology–Head and Neck Surgery, Volume 173, Issue 5, Page 1079-1091, November 2025.
Abstract Objective To evaluate the impact of mucosal grafts and flaps on neo‐ostium patency and clinical outcomes in patients undergoing Draf IIb or III frontal sinus drill‐out procedures. Data Sources A systematic search was conducted across PubMed, Medline, Cochrane Library, Scopus, and Web of Science databases in accordance with Preferred Reporting ...
Alexander Lein   +8 more
wiley   +1 more source

Nevus sebaceus with syringocystadenoma papilliferum, prurigo nodularis, apocrine cystadenoma, basaloid follicular proliferation, and sebaceoma: case report and review of nevus sebaceus-associated conditions [PDF]

open access: yes, 2020
Nevus sebaceus is a benign skin hamartoma of congenital onset that grows during puberty, and in adulthood can develop secondary benign and malignant neoplasms.
Basu, Pallavi   +3 more
core   +1 more source

APC‐related multiple salivary gland lesions: spatial transcriptomic analysis reveals progressive WNT activation

open access: yesThe Journal of Pathology, Volume 267, Issue 3, Page 241-248, November 2025.
Abstract Attenuated familial adenomatous polyposis (AFAP) is a disorder caused by germline pathogenic variants in APC and is characterized by the presence of <100 colonic polyps and a high lifetime risk of developing colorectal cancer. Salivary gland basal cell tumours are uncommon and have not previously been reported in AFAP. We present a family with
Fiona Chan‐Pak‐Choon   +12 more
wiley   +1 more source

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