Pineal choriocarcinoma

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sujit Routray, M.D. [2]

Synonyms and Keywords: Pineal embryonal cell carcinoma; Pineal gland tumor; Brain tumor


  • Pineal choriocarcinoma is a relatively rare, malignant, highly vascular neoplasm and accounts for a small proportion of all intracranial germ cell tumors. It is an aggressive tumor and has a propensity to metastasise systemically. Pure pineal choriocarcinoma tumors secrete β-HCG.[1]
  • On microscopic histopathological analysis, pineal choriocarcinoma is characterized by presence of intimately related syncytiotrophoblasts and cytotrophoblasts without formation of definite placental type villi. Syncytiotrophoblasts are large multi-nucleated cells with eosinophilic cytoplasm. They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in chorionic villi. Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm.[2]
  • Pineal choriocarcinoma accounts for 5% of all pineal masses.[1]
  • The peak age at diagnosis for pineal choriocarcinoma is 20-30 years.
  • Common complications of pineal choriocarcinoma include:[3][4]

Management of Pineal Choriocarcinoma

Management Options of Penial Gland tumors
CSF diversion
  • The optimal surgical strategy to treat acute hydrocephalus in patients with pineal tumors is uncertain.
  • CSF diversion (ventriculoperitoneal [VP] shunt or third ventriculostomy may be necessary in symptomatic patients, although debulking surgery may obviate the need for this procedure
  • When CSF diversion is necessary, endoscopic third ventriculostomy can be carried out at the same time as the biopsy and is preferred over VP shunts, which can be complicated by infection, shunt malfunction, subdural hematoma, and rarely, tumor seeding
Surgical resection
  • Some series report long-term survival with surgery alone, even in patients with pineoblastomas.
  • Indeed, for pineoblastomas, gross total surgical resection appears to correlate with improved survival.
  • Patients with symptomatic recurrent pineocytomas should also be considered for surgical resection of the lesion
  • Postoperative adjuvant RT is frequently (but not universally) recommended, and local control is dose-dependent.
  • The incidence of leptomeningeal recurrence was significantly lower among patients receiving CSI compared with those who did not.
  • The five-year survival rates were 86 and 49 percent for pineocytomas and non-pineocytoma PPTs, respectively.
  • Adjuvant RT is not universally recommended after gross total resection of a pineocytoma
Stereotactic radiosurgery
  • Stereotactic radiosurgery (SRS) is emerging as a useful treatment alternative for pineocytomas, although experience is limited.
  • The precise radiation fields that are defined by MRI or CT-computerized treatment planning minimize damage to the surrounding brain, and the risks of general anesthesia and craniotomy are avoided.
  • SRS is increasingly being used to treat pineal region tumors, either as an additional therapy after conventional treatments or as a primary treatment.
  • Due to the low rate of side effects, IRS may develop into an attractive alternative to microsurgery in de novo diagnosed pineocytomas. In malignant PPTs, IRS may be routinely applied in a multimodality treatment schedule supplementary to conventional irradiation.
Chemotherapy as part of multimodality therapy
  • The similarity of pineoblastomas to medulloblastomas in terms of their clinical behavior and tendency for leptomeningeal seeding has led to the use of similar chemotherapy regimens in patients with pineoblastoma as part of a multimodality approach.
  • Chemotherapy has been used to delay radiation therapy in very young children, for whom the long-term neurocognitive and developmental side effects of craniospinal irradiation (CSI) are a major concern.
  • The importance of radiation therapy as a component of the initial treatment of supratentorial primitive neuroectodermal tumors (PNETs) is also supported by the German HIT-SKK87 and HIT-SKK92 protocols, as well as the Canadian pediatric brain tumor protocol


  1. 1.0 1.1 Intracranial choriocarcinoma. Frank Gaillard et al. Radiopaedia 2015. Accessed on December 7, 2015
  2. Pathology of choriocarcinoma. Wikipedia 2015. Accessed on December 7, 2015
  3. Kida Y, Banno M, Kanzaki M, Kobayashi T, Kageyama N (1985). "[Pineal choriocarcinoma presenting massive ventricular hemorrhage--a case report]". No Shinkei Geka. 13 (6): 641–5. PMID 3840234.
  4. Radiographic features of intracranial choriocarcinoma. Frank Gaillard et al. Radiopaedia 2015. Accessed on December 7, 2015
  5. 5.0 5.1 5.2 5.3 Fujii, Toru; Itakura, Toru; Hayashi, Seiji; Komai, Norihiko; Nakamine, Hirokazu; Saito, Koji (1981). "Primary pineal choriocarcinoma with hemorrhage monitored by computerized tomography". Journal of Neurosurgery. 55 (3): 484–487. doi:10.3171/jns.1981.55.3.0484. ISSN 0022-3085.
  6. MRI brain radiographic features of intracranial choriocarcinoma. Frank Gaillard et al. Radiopaedia 2015. Accessed on December 8, 2015