Extragonadal germ cell tumor with the “burned-out” phenomenon presented a multiple retroperitoneal masses: a case report

retroperitoneal lymph node biopsy which revealed no evidence of malignancy, but detected 4–5 mm tumor necrosis foci in some areas. The patient followed by three cycles of chemotherapy with bleomycin, etoposide, and cisplatin protocol. Follow-up CT after chemotherapy revealed that the para-aortic lymphadenopathies had decreased in size to 3.4 cm × 2 cm × 1.6 cm. The patient then underwent a retroperitoneal lymph node dissection. Pathology result reported that the lymph nodes metastases of testicular germ cell tumor. Immunohistochemistry was positive for PLAP (focal), PANCK, HCG (focal), and CD117, and negative for AFP, HMB45, CD30, and CD45. Extragonadal germ cell tumors are rare and 5%–10% of all germ cell tumors, and they are predominantly affect young population.1 Extragonadal germ cell tumors are usually detected in the retroperitoneal, cervical, supraclavicular, and axillary lymph nodes and occasionally in the lung and liver. New epidemiologic study designed from Network of German Cancer Registries (GEKID) gave clue that extragonadal germ cell tumors usually appear not only mediastinal and retroperitoneal, but also in brain.2 Patients with retroperitoneal germ cell tumors usually detected lately after tumors getting larger to be a symptomatic. The symptoms are presented with a palpable mass, weight loss, constipation, back pain, dyspnea, leg edema, fever, and urinary retention. “Burned-out” phenomenon of testicular tumor is the spontaneous regression of a testicular germ cell tumor with or without metastasis. In our case report, we did not found the primary testicular tumor with histological characteristics of a germ cell tumor because of it was regressed after the development of metastasis in the retroperitoneum. There are two ways to explain “burned-out” phenomenon. The first one is spontaneous regression of the primary germ cell tumor after metastasis of the germ cell tumor. Possible mechanisms are an immune response or ischemia caused by the neoplasm disseminate due to its high metabolic rate. The second way is the de-novo development of a primary germ cell tumor in extragonadal tissues.3 Histological features of testicular specimen are helpful in establishing a diagnosis of a regressed testicular germ cell tumor include, apart from the scar formation, intratubular calcifications, lymphoplasmacytic infiltrate, hemosiderin-containing macrophages, and testicular atrophy.4 Due to burned-out tumors may cause some confusion in the diagnosis, careful examination of the testis is essential for identifying the primary lesion site; if suspect Dear Editor, Burned-out tumors of the testis are extremely rare form of testicular malignancies, and they could disappear or regress spontaneously and completely. These tumors could be presented by metastatic form in retroperitoneum, lungs, retroperitoneal lymph nodes, and liver. In recent studies, differential diagnosis, clinic features, treatment modalities and follow-up outcome of burned-out tumor from primary retroperitoneal germ cell tumor are discussed. If patient with retroperitoneal lymph node involvement and histology of “testicular tumor”, burned-out tumor of the testis was suspected. Although screening of scrotal contents may be useful to identify intratesticular abnormalities in these cases, radical orchidectomy should be performed if burned-out tumor were suspected. We present a case of a 39-year-old male complained of intermittent and increasing abdominal pain over the previous 2 months. The patient had no relevant past medical history. Abdominal examination revealed no palpable and tender mass. Scrotal examination revealed a normal left testis, but the right testis was atrophic, and no discrete mass was detected. Laboratory investigations were within normal ranges, with α-fetoprotein (AFP) 2.83 IU l−1 (0–9 IU l−1), β-human chorionic gonadotropin (HCG) hormone <0.1 IU l−1 (<0.1 IU l−1), and lactate dehydrogenase 183 IU l−1(100–190 IU l−1). Scrotal ultrasonography revealed a normal left testis and atrophic right testicle with heterogeneous architecture and scattered micro-calcifications which may result with postorchitis sequel. No mass was visualized. Abdominal computed tomography (CT) showed multiple retroperitoneal masses with hypodens and soft tissue components extending from below the bilateral renal arteries down to the bifurcation of the aorta. The biggest one of the lymph nodes was 6 cm × 4 cm × 3 cm in diameter (Figure 1). A right radical orchiectomy was performed. The testicular size was 6 cm × 3 cm, 5 cm × 2.5 cm. Histopathology showed subtotal atrophy of the testis due to collected with stromal degenerative collagenous deposits in testicular parenchyma. There was no evidence of germ cell tumor, and immunostains including placental alkaline phosphatase (PLAP), Masson-trichroma, Kongo-red, and Periodic acid Schiff were negative. The patient subsequently underwent a CT-guided LETTER TO THE EDITOR