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1.
Ann Otol Rhinol Laryngol ; 131(11): 1287-1292, 2022 Nov.
Article in English | MEDLINE | ID: mdl-34918575

ABSTRACT

OBJECTIVES: Congenital vascular lesions commonly present in the head and neck, and most are managed conservatively. Location and rapid growth, however, may necessitate surgical intervention. Endoscopic endonasal surgery (EES) in the pediatric population has emerged as a viable option in treating sinonasal and skull base lesions. Utilizing these techniques in newborns carries unique challenges. The objective of this report is to describe the successful use of direct intralesional embolization followed by endoscopic endonasal resection of a venous malformation in a postnatal patient. METHODS: We reviewed the case reported and reviewed the pertinent literature. RESULTS: A 6-week-old infant was found to have a large right-sided sinonasal lesion confirmed as a venous malformation. Rapid growth, impending orbital compromise, and potential long-term craniofacial abnormalities demanded the need for urgent surgical intervention. Risk of bleeding was mitigated with direct intralesional embolization. Immediately afterward, the patient underwent endoscopic endonasal resection of the lesion. EES in the very young presents multiple challenges both anatomically and behaviorally. A multidisciplinary approach lead to a successful outcome. CONCLUSION: We report a case of a 6-week-old infant, the youngest reported patient to the authors' knowledge, who successfully underwent direct intralesional embolization followed by endoscopic endonasal resection of a sinonasal vascular malformation. This report highlights the challenges of this technique in the very young and demonstrates it as a viable treatment strategy for sinonasal vascular anomalies in this population.


Subject(s)
Skull Base Neoplasms , Vascular Neoplasms , Child , Endoscopy/methods , Humans , Infant, Newborn , Magnetic Resonance Imaging , Skull Base/surgery , Skull Base Neoplasms/surgery
2.
Otolaryngol Clin North Am ; 54(3): 521-530, 2021 Jun.
Article in English | MEDLINE | ID: mdl-34024480

ABSTRACT

Duct scar in the form of stenoses or stricture is the second leading cause of obstructive sialadenitis after stone. Over the past decade, there has been a growing experience demonstrating the effectiveness of endoscopic techniques in the minimally invasive management of salivary duct stenosis. Less information, however, is available with regard to open approaches for recurrent or complex ductal stenoses. This article reports on a case of gland preservation using an open ductal technique that originally was applied in cases of traumatic Stensen's duct injury.


Subject(s)
Salivary Ducts , Sialadenitis , Cicatrix , Constriction, Pathologic , Endoscopy , Humans , Salivary Ducts/pathology , Salivary Ducts/surgery , Sialadenitis/pathology
3.
Sci Rep ; 8(1): 5808, 2018 04 11.
Article in English | MEDLINE | ID: mdl-29643359

ABSTRACT

The precise role of tumor associated macrophages remains unclear in pancreatic ductal adenocarcinoma (PDAC) while TGF-ß has an unclear role in metastases formation. In order to understand the role of IL23, an interleukin associated with macrophage polarization, we investigated IL23 in the context of TGF-ß expression in PDAC. We hypothesized that IL23 expression is associated with metastatic development and survival in PDAC. We investigated IL23 and TGF-ß protein expression on resected PDAC patient tumor sections who were divided into short-term (<12 months) survivors and long-term (>30 months) survivors. Panc-1 cells treated with IL23, TGF-ß, macrophages, or combinations thereof, were orthotopically implanted into NSG mice. Patients in the long-term survivor group had higher IL23 protein expression (P = 0.01). IL23 expression was linearly correlated with TGF-ß expression in patients in the short-term survivor group (P = 0.038). Macrophages induce a higher rate of PDAC metastasis in the mouse model (P = 0.02), which is abrogated by IL23 and TGF-ß treatment (P < 0.001). Macrophages serve a critical role in PDAC tumor growth and metastasis. TGF-ß contributes to a less tumorigenic TME through regulation of macrophages. Macrophages increases PDAC primary tumor growth and metastases formation while combined IL23 and TGF-ß pre-treatment diminishes these processes.


Subject(s)
Carcinoma, Pancreatic Ductal/pathology , Interleukin-23 Subunit p19/analysis , Macrophages/drug effects , Macrophages/immunology , Neoplasm Metastasis/prevention & control , Transforming Growth Factor beta/analysis , Aged , Animals , Disease Models, Animal , Humans , Immunohistochemistry , Mice , Middle Aged , Survival Analysis
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