A searchable database of
medically documented cases

About the Project

Spontaneous Regression Of Pineal Lesions: Ghost Tumor Or Pineal Apoplexy?

Mattogno et al., 2016Brain tumor

Mattogno, P. P., Frassanito, P., Massimi, L., Tamburrini, G., Novello, M., Lauriola, L., & Caldarelli, M. (2016). spontaneous Regression of Pineal Lesions: Ghost Tumor or Pineal Apoplexy?. World neurosurgery, 88, 64–69. https://doi.org/10.1016/j.wneu.2015.12.080

View Original Source →

Abstract

BACKGROUND: Pineal apoplexy (either hemorrhagic or ischemic) may complicate the course of a tumor at this site. This event usually is characterized by an acute clinical onset and requires emergency surgical management whereas the regression of the lesion is a much rarer outcome. MATERIAL AND METHODS: Three cases of pineal vanishing tumors in the pediatric population are reported and the pertinent literature is reviewed. RESULTS: In one case, radiologic findings were consistent with a diagnosis of pineal cyst, which became symptomatic after a spontaneous hemorrhage. This event may also explain its regression after the treatment of associated hydrocephalus. In the remaining 2 cases, neuroimaging examinations disclosed a solid tumor. One of them regressed after a surgical biopsy, probably because of an ischemic evolution, whereas the last one disappeared without any medical or surgical manipulation. Neither hemorrhage nor ischemia were noticed, thus the mechanism of regression remains controversial. CONCLUSIONS: Vanishing tumors of the pineal region may occur in different circumstances, resulting from absence of any medical and surgical action to minor manipulation of the tumor to obtain a biopsy. This variety may reflect different underlying mechanisms, leading to hemorrhagic or ischemic change of the tumor and its subsequent regression, although radiological imaging may fail to document hemorrhage or ischemia.

Case Details

Disease Location

Pineal gland

Personal Characteristics

12-year-old girl

Clinical Characteristics

12-year-old girl presenting with 2 months of nucal headache followed by nausea and vomiting. Head CT scan showed a hyperdense lesion of the quadrigeminal plate causing obstructive hydrocephalus. MRI confirmed a round mass, isointense on t1-weighted and t2-weighted images, with thin ring enhancement, consistent with a pineal cyst. The patient underwent endoscopic third ventriculostomy for the treatment of hydrocephalus.

Remission Characteristics

Early post-operative CT scan demonstrated the resolution of the hydrocephalus without changes of the cyst. The young girl had a complete resolution of preoperative symptoms. MRI performed 3 months later showed the complete disappearance of the cysts, which persists after a 5-year follow-up

Treatment & Mechanisms

Proposed Remission Mechanisms

Tumor apoplexy related to intracranial pressure drop

Clinical Treatment

Endoscopic third ventriculostomy for hydrocephalus

Non-Clinical Treatment

None reported