Gunsel Acikgoz
Hospital of the University of Pennsylvania
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Clinical Nuclear Medicine | 2007
Tevfik Cermik; Ayse Mavi; Gunsel Acikgoz; Mohamed Houseni; Simin Dadparvar; Abass Alavi
Purpose: The aim of this study was to assess the role of PET in the management of patients with primary malignant salivary gland (SG) tumor. Material and Methods: Sixty-one FDG PET studies in 48 patients (median age 58, range 28–89 years, 20 female, 28 male) who were diagnosed with malignant SG tumors were retrospectively analyzed. Thirteen were referred for initial diagnosis and staging while there was a suspicion of recurrence and/or metastatic disease in 48 patients during the follow-up period. Results: On PET examinations of 13 patients on initial presentation, 12 showed increased uptake in the primary lesion, while conventional methods (CT, MRI) were positive in 11 and were equivocal for 2 patients. Six patients with multiple nodal and 2 patients with distant metastases were detected by PET. Conventional methods demonstrated lymph node metastases in 5 of these patients. In the follow-up patient group, PET was inaccurate (false-negative or positive) in 4 (8%) patients with local recurrence, and in 4 (8%) with metastatic disease. However, 15 (31%) studies for recurrence and 7 (15%) for metastasis were false-negative with conventional radiologic methods. The sensitivity, specificity, and positive and negative predictive values for the detection of recurrent disease were 83%, 93%, 63%, and 98% for PET; 67%, 69%, 24%, and 94% for conventional methods, respectively. Overall sensitivity, specificity, positive and negative predictive values of PET for detecting metastatic disease were 93%, 96%, 82%, and 99%, while those of conventional methods were 80%, 95%, 75%, and 96%, respectively. Conclusion: These results demonstrate that FDG PET is not only superior to CT and/or MRI for staging at the initial presentation but also superior to conventional imaging methodologies for detecting local recurrence and regional lymph node and distant metastases in patients with malignant SG tumor.
Clinical Nuclear Medicine | 2006
Gunsel Acikgoz; Sung M. Kim; Mohamed Houseni; Tevfik Cermik; Charles M. Intenzo; Abass Alavi
The lungs are among the most common sites for metastases from a multitude of cancers. The majority of pulmonary metastases appear nodular on radiologic images. Interstitial spread of tumor through pulmonary lymphatics, also known as pulmonary lymphangitic carcinomatosis (PLC), is not uncommon and constitutes approximately 7% of pulmonary metastases. PLC is most often seen with adenocarcinoma of a variety of histologies such as thyroid carcinoma, and melanoma. It is usually noted in late stages of malignancy and therefore is indicative of a poor prognosis. Diagnosis of PLC is usually based on a combination of clinical and radiologic findings. However, the diagnosis is difficult when patients have limited clinical findings or have a history of or the possibility of other interstitial lung diseases. High-resolution computed tomography (HRCT) has been the modality of choice in the radiologic diagnosis of PLC. Imaging features of PLC on HRCT include thickening of interlobular septa, fissures, and bronchovascular bundles. Distribution of PLC may be focal or diffuse, unilateral or bilateral, and symmetric or asymmetric. Although FDG-PET has been extensively used in primary or secondary lung malignancies, its role and appearance in PLC have not been well determined in the literature. In this communication, we describe a spectrum of FDG-PET and CT findings in 5 cases with PLC. Similar to CT, the distribution of PLC can be extensive or limited on the FDG-PET. Diffuse, lobar, or segmental FDG uptake in the lungs is seen in extensive PLC. In limited PLC, a linear or a hazy area of FDG uptake extending from the tumor can be seen. Recognition of various patterns related to PLC on FDG-PET may allow accurate diagnosis of disease and could potentially influence the management of these patients.
Society of Nuclear Medicine Annual Meeting Abstracts | 2006
Gunsel Acikgoz; Mohamed Houseni; Mehdi Bathaii; Hua Yang; Wichana Chamroonrat; Abass Alavi
Society of Nuclear Medicine Annual Meeting Abstracts | 2006
Gunsel Acikgoz; Gonca Bural; Mohamed Houseni; Wichana Chamroonrat; Khaled Alkhawaldeh; Mehdi Bathaii; Abass Alavi
Society of Nuclear Medicine Annual Meeting Abstracts | 2006
Gunsel Acikgoz; Mohamed Houseni; Khaled Alkhawaldeh; Tevfik Cermik; Simin Dadparvar; Ayse Mavi; Abass Alavi
Society of Nuclear Medicine Annual Meeting Abstracts | 2007
Gonca Bural; Gunsel Acikgoz; Mohamed Houseni; Simin Dadparvar; Wichana Chamroonrat; Abass Alavi
Society of Nuclear Medicine Annual Meeting Abstracts | 2007
Gunsel Acikgoz; Tevfik Cermik; Gonca Bural; Mohamed Houseni; Abas Alavi
Society of Nuclear Medicine Annual Meeting Abstracts | 2007
Tevfik Cermik; Ayse Mavi; Gunsel Acikgoz; Simin Dadparvar; Abass Alavi
Society of Nuclear Medicine Annual Meeting Abstracts | 2007
Tevfik Cermik; Ayse Mavi; Gunsel Acikgoz; Simin Dadparvar; Abass Alavi
The Journal of Nuclear Medicine | 2006
Gonca Bural; Khaled Alkhawaldeh; Gunsel Acikgoz; Mohamed Houseni; Wichana Chamroonrat; Abass Alavi