A 60-year-old man who never smoked presented with a 2-month history of dull, poorly localized right-sided chest pain and a dry cough. He also reported a loss of appetite and unintentional weight loss. On clinical examination, he was hemodynamically stable, with clear breath sounds bilaterally. His hemogram and biochemical parameters were within normal limits, and electrocardiography showed a normal sinus rhythm. A posteroanterior chest radiograph revealed a suspicious mass lesion in the right upper zone. Contrast-enhanced computed tomography (CT) of the chest demonstrated a 70 mm × 40 mm × 61 mm spiculated, heterogeneously enhancing soft-tissue lesion in the apical segment of the right upper lobe. Whole-body 18F-fluorodeoxyglucose positron/emission tomography (FDG PET) showed avid uptake in the lesion (maximum standardized uptake value, 8.4), suggesting high metabolic activity consistent with malignancy. Radial endobronchial ultrasound (EBUS)-guided transbronchial lung biopsy was performed. Fiberoptic bronchoscopy showed no visible endobronchial growth. Biopsy specimens obtained under radial EBUS guidance yielded inconclusive histopathologic findings. A follow-up CT-guided percutaneous biopsy of the mass demonstrated necrotic material only, without viable tumor cells. The imaging features and metabolic activity were strongly suggestive of malignancy, yet repeated biopsy attempts failed to yield diagnostic tissue. The case underscores the diagnostic difficulty in sampling centrally necrotic tumors and the need for integrating imaging with clinical and histologic correlation.
60岁男性,从不吸烟,表现为2个月的钝性局限性右侧胸痛和干咳。他还报告说自己食欲不振,体重意外下降。临床检查,患者血流动力学稳定,双侧呼吸音清晰。他的血象和生化指标在正常范围内,心电图显示窦性心律正常。胸部后前方x光片显示右上区可疑肿块。胸部CT增强扫描显示右上肺叶顶端段一70 mm × 40 mm × 61 mm的多刺状软组织病变。全身18f -氟脱氧葡萄糖正电子发射断层扫描(FDG PET)显示病变部位摄取旺盛(最大标准化摄取值8.4),提示高代谢活性与恶性肿瘤一致。行桡骨支气管内超声引导下经支气管肺活检。纤维支气管镜未见支气管内生长。在径向EBUS引导下获得的活检标本产生不确定的组织病理学结果。随后的ct引导下的肿块经皮活检显示只有坏死物质,没有活的肿瘤细胞。影像特征和代谢活动强烈提示恶性肿瘤,但多次活检未能产生诊断组织。该病例强调了对中心坏死肿瘤取样诊断的困难,以及将影像学与临床和组织学相关性结合起来的必要性。
{"title":"PET/CT-Guided Biopsy in Necrotic Lung Mass: A Diagnostic Breakthrough.","authors":"Anurag Jain, Kunal Kumar, Divya Gupta, Vikrant Balaan, Neeraj Kumar, Madan Gopal Vishnoi, Abhishek Mahato","doi":"10.4103/ijnm.ijnm_66_25","DOIUrl":"10.4103/ijnm.ijnm_66_25","url":null,"abstract":"<p><p>A 60-year-old man who never smoked presented with a 2-month history of dull, poorly localized right-sided chest pain and a dry cough. He also reported a loss of appetite and unintentional weight loss. On clinical examination, he was hemodynamically stable, with clear breath sounds bilaterally. His hemogram and biochemical parameters were within normal limits, and electrocardiography showed a normal sinus rhythm. A posteroanterior chest radiograph revealed a suspicious mass lesion in the right upper zone. Contrast-enhanced computed tomography (CT) of the chest demonstrated a 70 mm × 40 mm × 61 mm spiculated, heterogeneously enhancing soft-tissue lesion in the apical segment of the right upper lobe. Whole-body <sup>18</sup>F-fluorodeoxyglucose positron/emission tomography (FDG PET) showed avid uptake in the lesion (maximum standardized uptake value, 8.4), suggesting high metabolic activity consistent with malignancy. Radial endobronchial ultrasound (EBUS)-guided transbronchial lung biopsy was performed. Fiberoptic bronchoscopy showed no visible endobronchial growth. Biopsy specimens obtained under radial EBUS guidance yielded inconclusive histopathologic findings. A follow-up CT-guided percutaneous biopsy of the mass demonstrated necrotic material only, without viable tumor cells. The imaging features and metabolic activity were strongly suggestive of malignancy, yet repeated biopsy attempts failed to yield diagnostic tissue. The case underscores the diagnostic difficulty in sampling centrally necrotic tumors and the need for integrating imaging with clinical and histologic correlation.</p>","PeriodicalId":45830,"journal":{"name":"Indian Journal of Nuclear Medicine","volume":"40 5","pages":"318-320"},"PeriodicalIF":0.5,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12633802/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589325","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-01Epub Date: 2025-10-31DOI: 10.4103/ijnm.ijnm_74_25
Anjali Meena, Karthikeyan Subramanian, Ashwani Sood, Bhagwant Rai Mittal
Metastasis from differentiated thyroid cancer frequently occurs in regional lymph nodes, followed by the lungs and bones. However, mandibular metastases related to thyroid carcinoma are exceedingly rare and may represent the sole manifestation of an undiagnosed underlying malignancy. This study aims to analyze the presentation, management, and survival outcomes in a case series of differentiated thyroid carcinoma patients having mandibular metastasis.
{"title":"Rare Presentation of Mandibular Metastases from Differentiated Thyroid Carcinoma: A Case Series - Experience from a Single Tertiary Care Hospital.","authors":"Anjali Meena, Karthikeyan Subramanian, Ashwani Sood, Bhagwant Rai Mittal","doi":"10.4103/ijnm.ijnm_74_25","DOIUrl":"10.4103/ijnm.ijnm_74_25","url":null,"abstract":"<p><p>Metastasis from differentiated thyroid cancer frequently occurs in regional lymph nodes, followed by the lungs and bones. However, mandibular metastases related to thyroid carcinoma are exceedingly rare and may represent the sole manifestation of an undiagnosed underlying malignancy. This study aims to analyze the presentation, management, and survival outcomes in a case series of differentiated thyroid carcinoma patients having mandibular metastasis.</p>","PeriodicalId":45830,"journal":{"name":"Indian Journal of Nuclear Medicine","volume":"40 5","pages":"304-308"},"PeriodicalIF":0.5,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12633808/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589431","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
<p><strong>Aim: </strong>To emphasize the feasibility of imaging prostate cancer patients under SPECT/CT with <sup>99m</sup>Tc-HYNIC-PSMA-11 and evaluate the possibility in clinical application for screening patients for radioligand therapy, with the help of SUV-based biodistribution mapping.</p><p><strong>Introduction: </strong>In context to prostate specific membrane antigen's (PSMA) overexpression in prostate cancer cells there has been a gradual increase in imaging prostate cancer, currently the second leading cause of cancer deaths in males and the sixth cause of cancer death worldwide, with the help of radiolabeled PSMA small molecule inhibitors over the past few years. Of the two modalities under Nuclear Medicine facility (positron emission tomography/CT [PET/CT] and single photon emission CT [SPECT/CT]), though PET/CT has high sensitivity for tumor sites, even at low PSA level less however, the availability of 18F based radiotracer for PET imaging necessitates the dependency on a cyclotron in the near vicinity for production or regular supply. Another option of Germanium 68/ Gallium 68 generator (<sup>68</sup>Ge/<sup>68</sup>Ga generator) can be explored but the cost involved becomes a limitation. These challenges led to the exploration of an alternative to help cater the needs of society with <sup>99m</sup>Tc labeled PSMA inhibitor, which is very easily available and a cost effective solution for imaging prostate cancer workup.</p><p><strong>Material and method: </strong>A retrospective analysis was conducted on 39 patients who had undergone <sup>99m</sup>Tc-HYNIC-PSMA-11 study over a period of 6 months. The patients were further categorized based on spread of disease and divided in two categories: localized disease and oligometastatic disease. Imaging was done under Discovery NM/CT 670 DR model SPECT/CT. The planar and SPECT/CT images were analyzed using Xeleris DR Functional imaging (Version 4.1) workstation under Q. Volumetric MI evolution for oncology software and maximum and mean standardized uptake value (SUV<sub>max</sub>, SUV<sub>mean</sub>) were determined on skeletal and soft tissue regions for both the categories (localized and oligometastatic). Further, statistical analysis was conducted through an independent samples t-test to find the significance, if any.</p><p><strong>Results: </strong>The biodistribution of <sup>99m</sup>Tc- HYNIC-PSMA-11 showed high uptake in parotid gland, submandibular gland, kidneys and urinary bladder, of which kidneys showed the highest uptake in all the scans. The SUV<sub>max</sub> and SUV<sub>mean</sub> comparison between localized and oligometastatic condition for various body regions did not show any statistically significant differences as indicted by the p-value.</p><p><strong>Conclusion: </strong>The biodistribution of <sup>99m</sup>Tc- HYNIC-PSMA-11 is similar to 68Ga-PSMA-11 scan, hence can be used as a cost-effective alternate for imaging overexpression of PSMA in case of prostate cancer
{"title":"Biodistribution and Semiquantitative Analysis of <sup>99m</sup>Tc-HYNIC-PSMA-11in Prostate Cancer Patients: A Retrospective Study.","authors":"Sachin Tayal, Ritwik Sinha, Varun Shukla, Manikandan Marappagounder Venkatachalam, Arvind Suresh, Jay Prakash Kumar, Manojkumar Ramsoorat Chauhan, Yash Jain, Uddeshya Narayan Jha, Simran Kalra","doi":"10.4103/ijnm.ijnm_45_25","DOIUrl":"10.4103/ijnm.ijnm_45_25","url":null,"abstract":"<p><strong>Aim: </strong>To emphasize the feasibility of imaging prostate cancer patients under SPECT/CT with <sup>99m</sup>Tc-HYNIC-PSMA-11 and evaluate the possibility in clinical application for screening patients for radioligand therapy, with the help of SUV-based biodistribution mapping.</p><p><strong>Introduction: </strong>In context to prostate specific membrane antigen's (PSMA) overexpression in prostate cancer cells there has been a gradual increase in imaging prostate cancer, currently the second leading cause of cancer deaths in males and the sixth cause of cancer death worldwide, with the help of radiolabeled PSMA small molecule inhibitors over the past few years. Of the two modalities under Nuclear Medicine facility (positron emission tomography/CT [PET/CT] and single photon emission CT [SPECT/CT]), though PET/CT has high sensitivity for tumor sites, even at low PSA level less however, the availability of 18F based radiotracer for PET imaging necessitates the dependency on a cyclotron in the near vicinity for production or regular supply. Another option of Germanium 68/ Gallium 68 generator (<sup>68</sup>Ge/<sup>68</sup>Ga generator) can be explored but the cost involved becomes a limitation. These challenges led to the exploration of an alternative to help cater the needs of society with <sup>99m</sup>Tc labeled PSMA inhibitor, which is very easily available and a cost effective solution for imaging prostate cancer workup.</p><p><strong>Material and method: </strong>A retrospective analysis was conducted on 39 patients who had undergone <sup>99m</sup>Tc-HYNIC-PSMA-11 study over a period of 6 months. The patients were further categorized based on spread of disease and divided in two categories: localized disease and oligometastatic disease. Imaging was done under Discovery NM/CT 670 DR model SPECT/CT. The planar and SPECT/CT images were analyzed using Xeleris DR Functional imaging (Version 4.1) workstation under Q. Volumetric MI evolution for oncology software and maximum and mean standardized uptake value (SUV<sub>max</sub>, SUV<sub>mean</sub>) were determined on skeletal and soft tissue regions for both the categories (localized and oligometastatic). Further, statistical analysis was conducted through an independent samples t-test to find the significance, if any.</p><p><strong>Results: </strong>The biodistribution of <sup>99m</sup>Tc- HYNIC-PSMA-11 showed high uptake in parotid gland, submandibular gland, kidneys and urinary bladder, of which kidneys showed the highest uptake in all the scans. The SUV<sub>max</sub> and SUV<sub>mean</sub> comparison between localized and oligometastatic condition for various body regions did not show any statistically significant differences as indicted by the p-value.</p><p><strong>Conclusion: </strong>The biodistribution of <sup>99m</sup>Tc- HYNIC-PSMA-11 is similar to 68Ga-PSMA-11 scan, hence can be used as a cost-effective alternate for imaging overexpression of PSMA in case of prostate cancer ","PeriodicalId":45830,"journal":{"name":"Indian Journal of Nuclear Medicine","volume":"40 5","pages":"269-277"},"PeriodicalIF":0.5,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12633813/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589272","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
We report a unique case of a patient with histopathologically proven diffuse large B-cell lymphoma (DLBCL) who underwent both 18F-fluorodeoxyglucose and 68Ga-Pentixafor positron emission tomography/computed tomography scans. The imaging findings showed an identical pattern of radiotracer uptake in disease-involved sites, including lymph nodes and extranodal sites. Despite the tracers having unrelated mechanisms, this concordance in imaging underscores the potential for complementary roles in disease staging, response evaluation, and theranostic applications in DLBCL cases exhibiting CXCR4 expression.
{"title":"Painted with the Same Brush: Identical PET/CT Scans in DLBCL Using Unrelated Tracers.","authors":"Pradap Palanivelu, Harish Goyal, Vasanth Madivanane, Prasanth Ganesan, Dhanapathi Halanaik","doi":"10.4103/ijnm.ijnm_157_24","DOIUrl":"10.4103/ijnm.ijnm_157_24","url":null,"abstract":"<p><p>We report a unique case of a patient with histopathologically proven diffuse large B-cell lymphoma (DLBCL) who underwent both <sup>18</sup>F-fluorodeoxyglucose and <sup>68</sup>Ga-Pentixafor positron emission tomography/computed tomography scans. The imaging findings showed an identical pattern of radiotracer uptake in disease-involved sites, including lymph nodes and extranodal sites. Despite the tracers having unrelated mechanisms, this concordance in imaging underscores the potential for complementary roles in disease staging, response evaluation, and theranostic applications in DLBCL cases exhibiting CXCR4 expression.</p>","PeriodicalId":45830,"journal":{"name":"Indian Journal of Nuclear Medicine","volume":"40 5","pages":"312-313"},"PeriodicalIF":0.5,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12633809/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589279","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Metastatic melanoma is the most life-threatening skin cancer due to its significant tendency to metastasize and its substantial resistance to therapeutic interventions. Melanomas spread aggressively, particularly to lymph nodes, the brain, and lungs, and can also involve the adrenal gland, liver, bones, and small intestine. Metastasis to the endometrium is exceedingly rare, with only a handful of documented cases. Fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) is an excellent modality for detecting metastases. A meta-analysis showed that PET/CT has superior diagnostic performance, with 88% sensitivity and 94% specificity, compared to other contemporary imaging techniques. We present a 55-year-old postmenopausal female, diagnosed with primary cutaneous melanoma of the right foot and initially treated with temozolomide. After 2 years, she presented with vaginal bleeding. Restaging with 18F FDG PET/CT revealed multiple nodal metastases with chest and abdominal wall deposits and confirmed uterine metastases.
{"title":"Navigating the Rare: <sup>18</sup>F FDG PET/CT Reveals Uterine Metastasis from Cutaneous Melanoma.","authors":"Ramya Subramani, Vivekanandhan Selvam, Vijay Singh, Selvaratnam Abhilash","doi":"10.4103/ijnm.ijnm_73_25","DOIUrl":"10.4103/ijnm.ijnm_73_25","url":null,"abstract":"<p><p>Metastatic melanoma is the most life-threatening skin cancer due to its significant tendency to metastasize and its substantial resistance to therapeutic interventions. Melanomas spread aggressively, particularly to lymph nodes, the brain, and lungs, and can also involve the adrenal gland, liver, bones, and small intestine. Metastasis to the endometrium is exceedingly rare, with only a handful of documented cases. Fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) is an excellent modality for detecting metastases. A meta-analysis showed that PET/CT has superior diagnostic performance, with 88% sensitivity and 94% specificity, compared to other contemporary imaging techniques. We present a 55-year-old postmenopausal female, diagnosed with primary cutaneous melanoma of the right foot and initially treated with temozolomide. After 2 years, she presented with vaginal bleeding. Restaging with <sup>18</sup>F FDG PET/CT revealed multiple nodal metastases with chest and abdominal wall deposits and confirmed uterine metastases.</p>","PeriodicalId":45830,"journal":{"name":"Indian Journal of Nuclear Medicine","volume":"40 5","pages":"309-311"},"PeriodicalIF":0.5,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12633810/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589366","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose of the study: This study compared striatal dopamine metabolism and cerebral glucose metabolism in Parkinson's disease patients with and without freezing of gait (FOG) using Fluorodeoxyglucose positron emission tomography (FDG-PET) and F-DOPA PET. We also compared the two groups' cognitive, affective, and autonomic functions.
Methods: Patients were divided into two groups: those with and without FOG. All patients underwent neuropsychological evaluation. Subsequently, both groups underwent FDG-PET and FDOPA-PET. The FDOPA PET/computed tomography images evaluated dopaminergic expression in the basal ganglia. Cortex-ID-based processing of FDG images was visually analyzed for any abnormal hypermetabolism or hypometabolism in the various regions of the brain.
Results: A total of 30 patients were recruited, 15 in each group. The mean age of participants was 59.33 ± 9.12 years in the freezing of the gait-negative group and 61.13 ± 9.38 years in the freezing of the gait-positive group. FDOPA PET scan analysis revealed symmetrical loss of basal ganglia uptake in the freezers compared to the nonfreezers, which had more asymmetrically reduced uptake (P = 0.025). In FDG PET, a general trend of greater metabolic reduction in the basal ganglia was observed in freezers. Our study showed bilateral involvement of frontoparietal cortices in both freezers and nonfreezers, with more widespread areas of hypometabolism reported in the freezer group.
Conclusion: Freezers exhibited a more symmetrical loss of dopaminergic uptake on FDOPA PET, whereas nonfreezers showed greater asymmetry. In addition, FDG PET revealed a trend toward greater basal ganglia hypometabolism in freezers, suggesting a more profound striatal dysfunction in patients with freezing of gait.
{"title":"Comparison of FDOPA and FDG PET in Parkinson's Disease Patients with and without Freezing of Gait.","authors":"Karthik Harisankar, Sahil Mehta, Rajender Kumar, Manju Mohanty, Jagdeep Singh, Shivangi Mehta, Shubh Mohan Singh, Kamalesh Chakravarty, Neeraj Balaini, Vivek Lal","doi":"10.4103/ijnm.ijnm_60_25","DOIUrl":"10.4103/ijnm.ijnm_60_25","url":null,"abstract":"<p><strong>Purpose of the study: </strong>This study compared striatal dopamine metabolism and cerebral glucose metabolism in Parkinson's disease patients with and without freezing of gait (FOG) using Fluorodeoxyglucose positron emission tomography (FDG-PET) and F-DOPA PET. We also compared the two groups' cognitive, affective, and autonomic functions.</p><p><strong>Methods: </strong>Patients were divided into two groups: those with and without FOG. All patients underwent neuropsychological evaluation. Subsequently, both groups underwent FDG-PET and FDOPA-PET. The FDOPA PET/computed tomography images evaluated dopaminergic expression in the basal ganglia. Cortex-ID-based processing of FDG images was visually analyzed for any abnormal hypermetabolism or hypometabolism in the various regions of the brain.</p><p><strong>Results: </strong>A total of 30 patients were recruited, 15 in each group. The mean age of participants was 59.33 ± 9.12 years in the freezing of the gait-negative group and 61.13 ± 9.38 years in the freezing of the gait-positive group. FDOPA PET scan analysis revealed symmetrical loss of basal ganglia uptake in the freezers compared to the nonfreezers, which had more asymmetrically reduced uptake (<i>P</i> = 0.025). In FDG PET, a general trend of greater metabolic reduction in the basal ganglia was observed in freezers. Our study showed bilateral involvement of frontoparietal cortices in both freezers and nonfreezers, with more widespread areas of hypometabolism reported in the freezer group.</p><p><strong>Conclusion: </strong>Freezers exhibited a more symmetrical loss of dopaminergic uptake on FDOPA PET, whereas nonfreezers showed greater asymmetry. In addition, FDG PET revealed a trend toward greater basal ganglia hypometabolism in freezers, suggesting a more profound striatal dysfunction in patients with freezing of gait.</p>","PeriodicalId":45830,"journal":{"name":"Indian Journal of Nuclear Medicine","volume":"40 5","pages":"290-295"},"PeriodicalIF":0.5,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12633811/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-01Epub Date: 2025-10-31DOI: 10.4103/ijnm.ijnm_71_25
Ikram Zahfir, Salah Nabih Oueriagli, Meryem Aboussabr, Omar Ait Sahel, Yassir Benameur, Abderrahim Doudouh
Hepatoid adenocarcinoma of the lung (HAL) is an exceptionally rare and highly aggressive form of extrahepatic adenocarcinoma. Characterized by alpha-fetoprotein production and exhibiting morphological features akin to hepatocellular carcinoma, it poses significant diagnostic and therapeutic challenges. We present the case of a 39-year-old male with a history of smoking, who sought medical attention for right-sided chest pain, cough, and difficulty breathing. Imaging studies, including a chest X-ray and ¹⁸F-FDG PET/CT scan, revealed a pulmonary mass with intense FDG uptake. Further pathological analysis confirmed the diagnosis of HAL, highlighting the importance of early recognition and accurate diagnosis of this rare malignancy.
{"title":"<sup>18</sup>F-FDG PET/CT in Lung Hepatoid Adenocarcinoma.","authors":"Ikram Zahfir, Salah Nabih Oueriagli, Meryem Aboussabr, Omar Ait Sahel, Yassir Benameur, Abderrahim Doudouh","doi":"10.4103/ijnm.ijnm_71_25","DOIUrl":"10.4103/ijnm.ijnm_71_25","url":null,"abstract":"<p><p>Hepatoid adenocarcinoma of the lung (HAL) is an exceptionally rare and highly aggressive form of extrahepatic adenocarcinoma. Characterized by alpha-fetoprotein production and exhibiting morphological features akin to hepatocellular carcinoma, it poses significant diagnostic and therapeutic challenges. We present the case of a 39-year-old male with a history of smoking, who sought medical attention for right-sided chest pain, cough, and difficulty breathing. Imaging studies, including a chest X-ray and ¹⁸F-FDG PET/CT scan, revealed a pulmonary mass with intense FDG uptake. Further pathological analysis confirmed the diagnosis of HAL, highlighting the importance of early recognition and accurate diagnosis of this rare malignancy.</p>","PeriodicalId":45830,"journal":{"name":"Indian Journal of Nuclear Medicine","volume":"40 5","pages":"314-315"},"PeriodicalIF":0.5,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12633803/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589270","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-01Epub Date: 2025-10-31DOI: 10.4103/ijnm.ijnm_44_25
Yeshwanth Edamadaka, Rahul V Parghane, Sandip Basu
The present report describes a patient of metastatic castration-resistant prostate cancer (mCRPC) with dural-based brain metastasis, discordant and variable [68Ga] Ga-prostate specific membrane antigen (PSMA)-11 and [18F] fluorodeoxyglucose ([18F] FDG) uptake in metastases on dual-tracer positron emission tomography computed tomography (PET/CT), illustrating three important teaching points: (a) Dual-tracer PET/CT demonstrating discordant tumor biology pattern between soft tissue and skeletal metastatic lesions in mCRPC even within the same individual, thereby provides a more comprehensive overview of whole-body tumor status, with implications for personalized patient profiling and treatment selection (b) valuable role of [18F] FDG-PET/CT in identifying PSMA-negative lesions (neuroendocrine transformation) in mCRPC patients, including the possibility of detecting second primary cancer, (c) high metabolic tumor volume on [18F] FDG-PET/CT associated with aggressive biology and adverse prognosis.
本文报道1例转移性去雄抵抗性前列腺癌(mCRPC)伴硬脑膜转移的患者,在双示踪正电子发射断层扫描(PET/CT)上发现转移灶中[68Ga] ga -前列腺特异性膜抗原(PSMA)-11和[18F]氟脱氧葡萄糖([18F] FDG)摄取不一致和可变,说明了三个重要的教学要点:(a)双示踪PET/CT显示即使在同一个体中,mCRPC中软组织和骨骼转移病变之间的肿瘤生物学模式也不一致,从而提供了更全面的全身肿瘤状态概述,对个性化患者分析和治疗选择具有重要意义(b) [18F] FDG-PET/CT在识别mCRPC患者psma阴性病变(神经内分泌转化)方面的重要作用。包括发现第二原发癌的可能性,(c) [18F] FDG-PET/CT上高代谢肿瘤体积与侵袭性生物学和不良预后相关。
{"title":"Tissue and Organ-specific Tumor Heterogeneity on dual tracer PET-CT ([<sup>68</sup>Ga] Ga-PSMA-11 and [<sup>18</sup>F] FDG) and Dural-based Brain metastasis in Metastatic Prostate Cancer.","authors":"Yeshwanth Edamadaka, Rahul V Parghane, Sandip Basu","doi":"10.4103/ijnm.ijnm_44_25","DOIUrl":"10.4103/ijnm.ijnm_44_25","url":null,"abstract":"<p><p>The present report describes a patient of metastatic castration-resistant prostate cancer (mCRPC) with dural-based brain metastasis, discordant and variable [<sup>68</sup>Ga] Ga-prostate specific membrane antigen (PSMA)-11 and [<sup>18</sup>F] fluorodeoxyglucose ([<sup>18</sup>F] FDG) uptake in metastases on dual-tracer positron emission tomography computed tomography (PET/CT), illustrating three important teaching points: (a) Dual-tracer PET/CT demonstrating discordant tumor biology pattern between soft tissue and skeletal metastatic lesions in mCRPC even within the same individual, thereby provides a more comprehensive overview of whole-body tumor status, with implications for personalized patient profiling and treatment selection (b) valuable role of [<sup>18</sup>F] FDG-PET/CT in identifying PSMA-negative lesions (neuroendocrine transformation) in mCRPC patients, including the possibility of detecting second primary cancer, (c) high metabolic tumor volume on [<sup>18</sup>F] FDG-PET/CT associated with aggressive biology and adverse prognosis.</p>","PeriodicalId":45830,"journal":{"name":"Indian Journal of Nuclear Medicine","volume":"40 5","pages":"301-303"},"PeriodicalIF":0.5,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12633800/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589438","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-01Epub Date: 2025-10-31DOI: 10.4103/ijnm.ijnm_30_25
Ziyi Yang, Jian Liu, Zhiqun Mao
Although gastric cancer is a prevalent malignant tumor worldwide, gastric cancer with bone marrow metastasis is rare and associated with extremely poor prognosis. The clinical manifestations of bone marrow metastasis are diverse and nonspecific, with diagnosis primarily confirmed through bone marrow biopsy. 18F fluorodeoxyglucose positron emission tomography/computed tomography (18F FDG PET/CT) serves as a sensitive modality for detecting bone marrow metastasis. We present a case of a female patient with gastric adenocarcinoma complicated by bone marrow metastasis, who presented with systemic pain and fatigue. 18F FDG PET/CT revealed metabolically active lesions in the vertebral column and multiple skeletal sites, while conventional CT showed no apparent signs of bone destruction.
{"title":"Gastric Adenocarcinoma with Bone Marrow Metastasis.","authors":"Ziyi Yang, Jian Liu, Zhiqun Mao","doi":"10.4103/ijnm.ijnm_30_25","DOIUrl":"10.4103/ijnm.ijnm_30_25","url":null,"abstract":"<p><p>Although gastric cancer is a prevalent malignant tumor worldwide, gastric cancer with bone marrow metastasis is rare and associated with extremely poor prognosis. The clinical manifestations of bone marrow metastasis are diverse and nonspecific, with diagnosis primarily confirmed through bone marrow biopsy. <sup>18</sup>F fluorodeoxyglucose positron emission tomography/computed tomography (<sup>18</sup>F FDG PET/CT) serves as a sensitive modality for detecting bone marrow metastasis. We present a case of a female patient with gastric adenocarcinoma complicated by bone marrow metastasis, who presented with systemic pain and fatigue. <sup>18</sup>F FDG PET/CT revealed metabolically active lesions in the vertebral column and multiple skeletal sites, while conventional CT showed no apparent signs of bone destruction.</p>","PeriodicalId":45830,"journal":{"name":"Indian Journal of Nuclear Medicine","volume":"40 5","pages":"296-298"},"PeriodicalIF":0.5,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12633804/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-01Epub Date: 2025-10-31DOI: 10.4103/ijnm.ijnm_87_25
Punit Sharma
{"title":"Is Terbium-161 the Next Lutetium-177? A New Era for Theranostics on the Horizon.","authors":"Punit Sharma","doi":"10.4103/ijnm.ijnm_87_25","DOIUrl":"10.4103/ijnm.ijnm_87_25","url":null,"abstract":"","PeriodicalId":45830,"journal":{"name":"Indian Journal of Nuclear Medicine","volume":"40 5","pages":"321-322"},"PeriodicalIF":0.5,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12633807/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589321","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}