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Published in: Journal of Neuro-Oncology 1/2008

01-10-2008 | Clinical-patient studies

Bifocal mixed germ-cell tumor with growing teratoma syndrome and metachronous mature metastases: case report

Authors: Johann Peltier, Matthieu Vinchon, Marc Baroncini, Olivier Kerdraon, Patrick Dhellemmes

Published in: Journal of Neuro-Oncology | Issue 1/2008

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Abstract

The authors report the case of a 16-year-old male who presented with a bifocal diencephalic tumor arising both in the neurohypophysis and the pineal region with hydrocephalus. The histological diagnosis obtained during endoscopic ventriculocisternostomy was germinoma. MRI revealed an increase of the neoplasm during chemotherapy with recurrent obstructive hydrocephalus. A new ventriculostomy was performed followed by total surgical resection. The final histopathological analysis demonstrated an immature teratoma. Subsequently, this patient developed metachronous cystic metastases in the cerebello-pontine angles, which were resected and identified as mature teratoma, then we observed a lesion of the brachium conjunctivum which stayed stable after 29 consecutive months. The patient is alive and feels well 6 years after the initial diagnosis and 5 years after the first metastasis. To our knowledge, this is the fifth case of the growing teratoma syndrome located in the brain but the first case with simultaneously bifocal location and infratentorial disseminated metastasis. Obviously surgical removal is the treatment of reference for teratomas. Metastases of teratoma can be mature and may be amenable to surgery with a favorable outcome. Primary intracranial germ-cell tumors (CGT) arise in the midline of the brain and are located in the diencephalon. The peak incidence occurs during the second decade of life. Germ cell tumor (CGT) includes germinomas and non-germinomatous tumors, mature and immature teratomas account for 19.6 % [1]. Curiously, teratomas are able to grow during the first weeks of chemotherapy while serum markers remain normal. This situation was originally described and designed as “the growing teratoma syndroma” (GTS) in primary testis tumors by Logothetis in 1982 [2]. Here we report the rare occurrence of a GTS in a teenager who presented metachronous cystic metastases located in posterior fossa which were histologically mature.
Literature
1.
go back to reference Matsutani M, Sano K, Takakura K, Fujimaki T, Nakamura O, Funata N, Seto T (1997) Intracranial germ-cell tumors in children. J Neurosurg 86:446–455CrossRefPubMed Matsutani M, Sano K, Takakura K, Fujimaki T, Nakamura O, Funata N, Seto T (1997) Intracranial germ-cell tumors in children. J Neurosurg 86:446–455CrossRefPubMed
2.
go back to reference Logothetis CJ, Samuels ML, Trindade A, Johnson DE (1982) The growing teratoma syndrome. Cancer 50:1629–1635CrossRefPubMed Logothetis CJ, Samuels ML, Trindade A, Johnson DE (1982) The growing teratoma syndrome. Cancer 50:1629–1635CrossRefPubMed
3.
go back to reference Bi WL, Bannykh SI, Baehring J (2005) The growing teratoma syndrome after subtotal resection of an intracranial nongerminatous germ cell tumor in an adult: case report. Neurosurgery 56:188PubMed Bi WL, Bannykh SI, Baehring J (2005) The growing teratoma syndrome after subtotal resection of an intracranial nongerminatous germ cell tumor in an adult: case report. Neurosurgery 56:188PubMed
4.
go back to reference Hoffman HJ, Otsubo H, Hendrick B, Humphreys RP, Drake JM, Becker LE et al (1991) Primary intracranial germ cell tumors: a clinical analysis of 153 histogically verified cases. J Neurosurg 74:545–551CrossRefPubMed Hoffman HJ, Otsubo H, Hendrick B, Humphreys RP, Drake JM, Becker LE et al (1991) Primary intracranial germ cell tumors: a clinical analysis of 153 histogically verified cases. J Neurosurg 74:545–551CrossRefPubMed
5.
go back to reference Russell WO, Sachs E (1943) Pinealomas: a clinicopathological study of seven cases with a review of the literature. Arch Pathol 35:869–888 Russell WO, Sachs E (1943) Pinealomas: a clinicopathological study of seven cases with a review of the literature. Arch Pathol 35:869–888
6.
go back to reference Friedman JA, Jynch JJ, Buckner JC, Scheithauer BW, Raffel C (2001) Management of malignant pineal germ cell tumors with residual mature teratoma. Neurosurgery 48:518–523CrossRefPubMed Friedman JA, Jynch JJ, Buckner JC, Scheithauer BW, Raffel C (2001) Management of malignant pineal germ cell tumors with residual mature teratoma. Neurosurgery 48:518–523CrossRefPubMed
7.
go back to reference Hanna A, Edan C, Heresbach N, Ben Hassel M, Guegan Y (2000) Expanding mature pineal teratoma syndrome: case report [in french]. Neurochirurgie 46:568–572PubMed Hanna A, Edan C, Heresbach N, Ben Hassel M, Guegan Y (2000) Expanding mature pineal teratoma syndrome: case report [in french]. Neurochirurgie 46:568–572PubMed
8.
go back to reference O’Callaghan AM, Katapodis O, Ellison DW, Theaker JM, Mead GM (1997) The growing teratoma syndrome in a nongerminatous germ cell tumor of the pineal gland. Cancer 80:942–947CrossRefPubMed O’Callaghan AM, Katapodis O, Ellison DW, Theaker JM, Mead GM (1997) The growing teratoma syndrome in a nongerminatous germ cell tumor of the pineal gland. Cancer 80:942–947CrossRefPubMed
9.
go back to reference Rustin GJ, Newlands SE, Bagshawe KD, Begent RHJ, Crawford SM (1986) Successful management of metastatic and primary germ cell tumors in the brain. Cancer 57:2108–2113CrossRefPubMed Rustin GJ, Newlands SE, Bagshawe KD, Begent RHJ, Crawford SM (1986) Successful management of metastatic and primary germ cell tumors in the brain. Cancer 57:2108–2113CrossRefPubMed
10.
go back to reference Andre F, Fizazi K, Culine S, Droz J, Taupin P, Lhomme C et al (2000) The growing teratoma syndrome: results of therapy and long term follow-up of 33 patients. Eur J Cancer 36:1389–1394CrossRefPubMed Andre F, Fizazi K, Culine S, Droz J, Taupin P, Lhomme C et al (2000) The growing teratoma syndrome: results of therapy and long term follow-up of 33 patients. Eur J Cancer 36:1389–1394CrossRefPubMed
11.
go back to reference Herrmann HD, Westphal M, Winkler K, Laas RW, Schulte FJ (1994) Treatment of nongerminatous germ-cell tumors of the pineal region. Neurosurgery 34:524–528CrossRefPubMed Herrmann HD, Westphal M, Winkler K, Laas RW, Schulte FJ (1994) Treatment of nongerminatous germ-cell tumors of the pineal region. Neurosurgery 34:524–528CrossRefPubMed
12.
go back to reference Lee AC, Chan GC, Fung CF, Leung SY, Lau YL (1995) Paradoxical response of a pineal immature teratoma to combination chemotherapy. Med Pediatr Oncol 24:53–57CrossRefPubMed Lee AC, Chan GC, Fung CF, Leung SY, Lau YL (1995) Paradoxical response of a pineal immature teratoma to combination chemotherapy. Med Pediatr Oncol 24:53–57CrossRefPubMed
13.
go back to reference Ueki K, Tanaka R (1980) Treatment and prognosis of pineal tumors-experience with 110 cases. Neurol Med Chir 20:1–26CrossRef Ueki K, Tanaka R (1980) Treatment and prognosis of pineal tumors-experience with 110 cases. Neurol Med Chir 20:1–26CrossRef
14.
go back to reference Teilum G (1965) Classification of endodermal sinus tumor and so-called “embryonal carcinoma” of the ovary. Acta Pathol Microbiol Scand 64:407–429PubMed Teilum G (1965) Classification of endodermal sinus tumor and so-called “embryonal carcinoma” of the ovary. Acta Pathol Microbiol Scand 64:407–429PubMed
15.
go back to reference Wara WM, Jenkin RD, Evans A, Ertel I, Hittle R, Ortega J, Wilson CB, Hammond D (1979) Tumors of the pineal and suprasellar region: Children’s Cancer Study Group treatment results 1960–1975. A report from the Children’s Cancer Study Group. Cancer 43:698–701CrossRefPubMed Wara WM, Jenkin RD, Evans A, Ertel I, Hittle R, Ortega J, Wilson CB, Hammond D (1979) Tumors of the pineal and suprasellar region: Children’s Cancer Study Group treatment results 1960–1975. A report from the Children’s Cancer Study Group. Cancer 43:698–701CrossRefPubMed
16.
go back to reference Sawamura Y, Kato T, Ikeda J, Murata J, Tada M, Shirato H (1988) Teratomas of the central nervous system: treatment considerations based on 34 cases. J Neurosurg 89:728–737 Sawamura Y, Kato T, Ikeda J, Murata J, Tada M, Shirato H (1988) Teratomas of the central nervous system: treatment considerations based on 34 cases. J Neurosurg 89:728–737
17.
go back to reference Graziano SL, Paolozzi FP, Rudolph AR, Stewart WA, Elbadawi A, Comis RL (1987) Mixed germ-cell tumor of the pineal region. J Neurosurg 66:300–304CrossRefPubMed Graziano SL, Paolozzi FP, Rudolph AR, Stewart WA, Elbadawi A, Comis RL (1987) Mixed germ-cell tumor of the pineal region. J Neurosurg 66:300–304CrossRefPubMed
18.
go back to reference Hirano T, Kumabe T, Murakami K, Watanabe M, Shirane R, Yoshimoto T (2001) Metachronous neurohypophysial immature teratoma occurring 10 years after total resection of pineal mature teratoma. Child’s Nerv Syst 17:286–289CrossRef Hirano T, Kumabe T, Murakami K, Watanabe M, Shirane R, Yoshimoto T (2001) Metachronous neurohypophysial immature teratoma occurring 10 years after total resection of pineal mature teratoma. Child’s Nerv Syst 17:286–289CrossRef
19.
go back to reference Weiner HL, Finlay JL (1999) Surgery in the management of primary intracranial germ cell tumors. Child’s Nerv Syst 15:770–773CrossRef Weiner HL, Finlay JL (1999) Surgery in the management of primary intracranial germ cell tumors. Child’s Nerv Syst 15:770–773CrossRef
20.
go back to reference Jeffery GM, Theaker JM, Lee AH, Blaquiere JM, Smart CJ, Mead GM (1991) The growing teratoma syndrome. Br J Urol 67:195–202CrossRefPubMed Jeffery GM, Theaker JM, Lee AH, Blaquiere JM, Smart CJ, Mead GM (1991) The growing teratoma syndrome. Br J Urol 67:195–202CrossRefPubMed
21.
go back to reference Simmonds PD, Mead GM, Whitehouse JM (1995) A complicated case of metastatic teratoma. Growing teratoma syndrome and cerebral metastasis. Ann Oncol 6:181–185PubMed Simmonds PD, Mead GM, Whitehouse JM (1995) A complicated case of metastatic teratoma. Growing teratoma syndrome and cerebral metastasis. Ann Oncol 6:181–185PubMed
22.
go back to reference Ornadel D, Wilson A, Trask C, Ledermann J (1995) Remission of recurrent mature teratoma with interferon therapy. J R Soc Med 88:533–534 Ornadel D, Wilson A, Trask C, Ledermann J (1995) Remission of recurrent mature teratoma with interferon therapy. J R Soc Med 88:533–534
Metadata
Title
Bifocal mixed germ-cell tumor with growing teratoma syndrome and metachronous mature metastases: case report
Authors
Johann Peltier
Matthieu Vinchon
Marc Baroncini
Olivier Kerdraon
Patrick Dhellemmes
Publication date
01-10-2008
Publisher
Springer US
Published in
Journal of Neuro-Oncology / Issue 1/2008
Print ISSN: 0167-594X
Electronic ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-008-9640-3

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