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 Table of Contents     
CASE REPORT
Year : 2016  |  Volume : 31  |  Issue : 3  |  Page : 204-206  

Late metastatic recurrence of penile carcinoma after 10 years: Demonstration with 18F-fluorodeoxyglucose positron emission tomography/computed tomography


Department of Nuclear Medicine and Positron Emission Tomography/Computed Tomography, Apollo Gleneagles Hospitals, Kolkata, West Bengal, India

Date of Web Publication7-Jun-2016

Correspondence Address:
Punit Sharma
13 Canal Circular Road, Kolkata - 700 054, West Bengal
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0972-3919.183611

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   Abstract 


Penile cancer is rare cancer. While inguinal and pelvic nodal metastasis is common, distant metastasis is rare. We here present the interesting case of a 59-year-old male patient with penile carcinoma, previously treated with penectomy and inguinal lymphadenectomy 10 years earlier. He presented with bone pains and given history of malignancy he was referred for an 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography/computed tomography (PET/CT). PET/CT demonstrated multiple 18F-FDG avid bone and lung metastases. No locoregional disease was seen. Biopsy from a lung nodule confirmed the diagnosis, and the patient was started on palliative chemotherapy.

Keywords: 18F-fluorodeoxyglucose, penile carcinoma, positron emission tomography/computed tomography, recurrence


How to cite this article:
Sharma P. Late metastatic recurrence of penile carcinoma after 10 years: Demonstration with 18F-fluorodeoxyglucose positron emission tomography/computed tomography. Indian J Nucl Med 2016;31:204-6

How to cite this URL:
Sharma P. Late metastatic recurrence of penile carcinoma after 10 years: Demonstration with 18F-fluorodeoxyglucose positron emission tomography/computed tomography. Indian J Nucl Med [serial online] 2016 [cited 2019 Dec 15];31:204-6. Available from: http://www.ijnm.in/text.asp?2016/31/3/204/183611




   Introduction Top


Penile cancer is relatively rare, representing about 0.5% of all male cancers.[1] It has a higher prevalence in developing countries and older men. Various predisposing factors include some religious and cultural practices, personal hygiene, smoking, phimosis, inflammatory conditions such as lichen sclerosus or balanoposthitis, ultraviolet radiation, and the presence of human papillomavirus.[2] Circumcision before puberty reduces the risk by 3–4 times.[2] Squamous-cell carcinoma (SCC) is the major histopathological subtype accounting for 95% of all penile cancers.[3] Regional nodes (inguinal and iliac) are the most common site of metastases. Distant metastasis to retroperitoneal nodes is still common, but to other sites such as lung, liver, and bones are rare.[4] Recurrence is commonly locoregional and usually appears within 2 years of primary treatment.[5] Distant recurrence is rare affecting only 1.8% of patients in one series.[5]18 F-fluorodeoxyglucose (18 F-FDG) positron emission tomography/computed tomography (PET/CT) has shown promising role in the nodal stating of penile cancer.[6] Here, we present a rare case of late recurrence (after a decade) of previously treated penile carcinoma presenting with distant metastases.


   Case Report Top


A 59-year-old male patient presented with multiple bone pains of 3 months duration. He was a follow-up case of penile cancer (SCC-G2; T2N2M0-Stage IIIB) for which he had undergone penectomy and bilateral inguinal nodal dissection 10 years back. This was followed by locoregional radiation. The patient was well for next 5 years but lost to follow-up thereafter. He was a chronic smoker. No other co-morbidity was present. The bone pains were not relieved with pain killers. Given history of malignancy, he was advised for 18 F-FDG PET/CT. Contrast enhanced 18 F-FDG PET/CT was performed after intravenous injection of 370 MBq (10 mCi) of 18 F-FDG. PET/CT images [Figure 1]a,[Figure 1]c,[Figure 1]d,[Figure 1]e showed multiple pulmonary (maximum standardized uptake value [SUVmax-6.2]) and bone metastases (SUVmax-11.3). No locoregional disease was seen. No other hypermetabolic lesion was seen in the body which would suggest a second primary tumor. Based on PET/CT findings, a diagnosis of metastatic relapse of penile cancer was made. However, given the long disease-free interval, a possibility of a second primary with metastases was considered by the treating oncologist. Biopsy from a pulmonary nodule was done which showed SCC, negative for thyroid transcription factor-1. Finally, a diagnosis of metastases from penile cancer was made. The patient was started on palliative chemotherapy with cisplatin and 6-flurouracil.
Figure 1: Maximum intensity projection positron emission tomography image. (a) Multiple hypermetabolic foci in thorax, abdomen and pelvis. Transaxial positron emission tomography/computed tomography image of pelvis (b) Postpenectomy status (arrow). No hypermetabolic lesion is seen in the penile stump, and no hypermetabolic inguinal node was seen. Transaxial positron emission tomography/computed tomography image of thorax. (c) Hypermetabolic pulmonary nodules (arrow). Furthermore, seen were multiple hypermetabolic lesions in multiple bones (d and e, arrows). Positron emission tomography/computed tomography findings suggested multiple skeletal and pulmonary metastases

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   Discussion Top


Penile cancer is usually locoregionally confined with distant spread seen only in advanced disease and is relatively rare. In the present case, the patient was demonstrated to have multiple distant metastases to lungs and bones on 18 F-FDG PET/CT. While recurrence in penile cancer is not uncommon, presentation as distant relapse is very rare.[4] Another interesting finding was the late presentation of the relapse, 10 years after primary treatment. Usually, recurrence in penile cancer is seen within 2 years of primary treatment.[5]

The role of 18 F-FDG PET/CT in penile cancer is still not clearly delineated. Many studies have evaluated its role in nodal staging with variable success. A meta-analysis including seven studies addressed the accuracy of 18 F-FDG PET/CT for inguinal lymph node staging in penile SCC.[6] It was found that the pooled sensitivity and specificity were 80.9% (95% confidence interval [CI]: 69.5–89.4%) and 92.4% (95% CI: 86.8–96.2%), respectively. Pooled sensitivity was 96.4% (95% CI: 81.7–99.9%) for clinically node-positive patients, and 56.5% (95% CI: 34.5–76.8%) for clinically node-negative patients. Based on these findings, the authors advised against the routine use of 18 F-FDG PET/CT in clinically node-negative patients, while PET/CT was thought to be useful in clinically node-positive patients. Similar results were also reported by Scher et al.[7] Another utility of PET/CT is detection of pelvic nodal metastasis in inguinal node-positive patients. Graafland et al.[8] showed a sensitivity of 91% and a specificity of 100% in detecting pelvic nodal involvement in 18 patients with penile SCC with unilateral or bilateral cytologically tumor-positive inguinal disease. A recent study by Jakobsen et al.[9] suggested that a combination of sentinel node biopsy and 18 F-FDG PET/CT to be more accurate than either alone in clinically inguinal node-negative penile cancer. In that study, four of 23 radiotracer-silent groins had an 18 F-FDG PET/CT positive node.

Although distant metastasis from penile cancer is rare, when present 18 F-FDG PET/CT can detect them with high sensitivity. Kaya et al.[10] Reported a case where distant nodal metastases from penile carcinoma were detected on a staging PET/CT done after primary surgery. Similarly, distant metastases were also demonstrated in few patients on 18 F-FDG PET/CT in various other studies.[7],[8],[9]18 F-FDG PET/CT being a whole body imaging technique is useful in this regard. In the present case too, PET/CT demonstrated multiple bone and lung metastases, reaffirming its utility.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Barnholtz-Sloan JS, Maldonado JL, Pow-sang J, Giuliano AR. Incidence trends in primary malignant penile cancer. Urol Oncol 2007;25:361-7.  Back to cited text no. 1
    
2.
Misra S, Chaturvedi A, Misra NC. Penile carcinoma: A challenge for the developing world. Lancet Oncol 2004;5:240-7.  Back to cited text no. 2
    
3.
Burgers JK, Badalament RA, Drago JR. Penile cancer. Clinical presentation, diagnosis, and staging. Urol Clin North Am 1992;19:247-56.  Back to cited text no. 3
    
4.
Sonpavde G, Pagliaro LC, Buonerba C, Dorff TB, Lee RJ, Di Lorenzo G. Penile cancer: Current therapy and future directions. Ann Oncol 2013;24:1179-89.  Back to cited text no. 4
    
5.
Leijte JA, Kirrander P, Antonini N, Windahl T, Horenblas S. Recurrence patterns of squamous cell carcinoma of the penis: Recommendations for follow-up based on a two-centre analysis of 700 patients. Eur Urol 2008;54:161-8.  Back to cited text no. 5
    
6.
Sadeghi R, Gholami H, Zakavi SR, Kakhki VR, Horenblas S. Accuracy of 18F-FDG PET/CT for diagnosing inguinal lymph node involvement in penile squamous cell carcinoma: Systematic review and meta-analysis of the literature. Clin Nucl Med 2012;37:436-41.  Back to cited text no. 6
    
7.
Scher B, Seitz M, Reiser M, Hungerhuber E, Hahn K, Tiling R, et al.18F-FDG PET/CT for staging of penile cancer. J Nucl Med 2005;46:1460-5.  Back to cited text no. 7
    
8.
Graafland NM, Leijte JA, Valdés Olmos RA, Hoefnagel CA, Teertstra HJ, Horenblas S. Scanning with 18F-FDG-PET/CT for detection of pelvic nodal involvement in inguinal node-positive penile carcinoma. Eur Urol 2009;56:339-45.  Back to cited text no. 8
    
9.
Jakobsen JK, Alslev L, Ipsen P, Costa JC, Krarup KP, Sommer P, et al. DaPeCa-3: Promising results of sentinel node biopsy combined with 18F-fluorodeoxyglucose positron emission tomography/computed tomography in clinically lymph node-negative patients with penile cancer – A national study from Denmark. BJU Int 2015. doi: 10.1111/bju.13243. [Epub ahead of print].  Back to cited text no. 9
    
10.
Kaya ZR, Sager S, Halac M, Sonmezoglu K. Disseminated metastatic penile squamous cell carcinoma detected by fluorodeoxyglucose PET/computerized tomography. Indian J Nucl Med 2012;27:189-91.  Back to cited text no. 10
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