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2.
Int J Surg Pathol ; 31(2): 124-136, 2023 Apr.
Article in English | MEDLINE | ID: mdl-35404169

ABSTRACT

Background. The sinonasal tract is the second most common site of human papillomavirus (HPV)-related carcinomas in the head and neck. Published data on the association between sinonasal tumors and HPV are quite inconsistent among different regions. Material and methods. We performed high-risk HPV DNA in situ hybridization (ISH) and p16 immunohistochemistry on sinonasal carcinomas diagnosed between 2006 and 2016. Results. Of 105 sinonasal carcinomas, we found only two (2%) HPV-positive cases; both had non-keratinizing morphology and were diffusely positive for p16. By histologic type, HPV DNA positivity rate was 14% in non-keratinizing squamous cell carcinomas, and we did not detect HPV DNA in any other type of sinonasal carcinomas. Thirteen HPV-negative tumors (7 salivary gland carcinomas, 3 sinonasal undifferentiated carcinomas, 2 keratinizing squamous cell carcinomas, and 1 non-keratinizing squamous cell carcinoma) were positive for p16. In nine carcinomas arising from an underlying sinonasal papilloma, p16 and HPV DNA ISH were evaluated in both carcinoma and papilloma areas and all were negative. Follow-up information was available for 104 patients; 46 (44%) were alive and 58 (55%) died of disease. One of the two HPV-positive patients died of the disease; the other was alive at 100 months of follow-up. Conclusions. We detected a much lower percentage of HPV positivity in sinonasal carcinomas when compared to the literature. We believe that our results support various rates of HPV-related carcinomas depending on the geographic and ethnic characteristics.


Subject(s)
Carcinoma, Squamous Cell , Maxillary Sinus Neoplasms , Papilloma , Papillomavirus Infections , Humans , Papillomavirus Infections/complications , Papillomavirus Infections/epidemiology , Papillomavirus Infections/pathology , Carcinoma, Squamous Cell/pathology , Risk Factors , Cyclin-Dependent Kinase Inhibitor p16/genetics
3.
Clin Nucl Med ; 47(3): e296-e297, 2022 Mar 01.
Article in English | MEDLINE | ID: mdl-35025778

ABSTRACT

ABSTRACT: We present the case of a 48-year-old man diagnosed with metastatic Ewing sarcoma who was referred for 18F-FDG PET/CT for treatment response evaluation following chemoradiotherapy. The patient also had complaints of new-onset testicular swelling at the time of imaging. Although the metastatic bone disease showed a complete metabolic response to treatment, 18F-FDG PET/CT demonstrated significantly increased metabolic activity in bilateral testicular mass. Consequently, the patient underwent bilateral orchiectomy, and histopathologic examination revealed bilateral testicular plasmacytoma, a rare manifestation of extramedullary plasmacytoma.


Subject(s)
Plasmacytoma , Sarcoma, Ewing , Fluorodeoxyglucose F18 , Humans , Male , Middle Aged , Plasmacytoma/diagnostic imaging , Positron Emission Tomography Computed Tomography , Positron-Emission Tomography
5.
Clin Nucl Med ; 46(12): e563-e564, 2021 Dec 01.
Article in English | MEDLINE | ID: mdl-34269725

ABSTRACT

ABSTRACT: 68Ga-Pentixafor is a novel radiotracer for imaging chemokine receptor subtype 4 (CXCR4) receptors, which are expressed exceptionally high in several hematologic malignancies, including various types of lymphoma. Herein we report a case of a 64-year-old man patient with suspected hematologic malignancy who underwent 18F-FDG and 68Ga-pentixafor PET/CT. Both scans demonstrated diffusely increased activity related to bone marrow involvement. 68Ga-Pentixafor PET/CT demonstrated CXCR4-expressing intra-abdominal lymph nodes that were not detected by 18F-FDG PET/CT. The patient was highly suspicious of lymphoma; however, histopathological examination of the bone marrow revealed systemic mastocytosis with associated myelofibrosis.


Subject(s)
Coordination Complexes , Lymphoma , Mastocytosis, Systemic , Humans , Lymphoma/diagnostic imaging , Male , Mastocytosis, Systemic/diagnostic imaging , Middle Aged , Peptides, Cyclic , Positron Emission Tomography Computed Tomography , Receptors, CXCR4
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