Metastatic craniopharyngioma: case report and literature review.

Childs Nerv Syst

Division of Neurosurgery, University of Saskatchewan, 103 Hospital Drive, Saskatoon, SK S7K 0W8, Canada.

Published: September 2009

Background: Distant spread of craniopharyngioma is a rare but important complication. Most cases are a result of spread along the surgical path. We describe a rare case of metastatic leptomeningeal craniopharyngioma as a result of dissemination along CSF pathways in a child. A review of previously described cases is provided.

Case Presentation: A 14-year-old male was diagnosed with metastatic craniopharyngioma on routine follow-up imaging after multiple surgeries and radiation for locally recurrent craniopharyngioma. The lesion was erosive through the right parietal bone, but had remained clinically silent. The lesion was distant from previous surgical paths. The patient underwent right parietal craniotomy and resection of the lesion. Duraplasty and cranioplasty were necessary for closure. Histopathology confirmed adamantinomatous craniopharyngioma. One-year follow-up demonstrated no recurrence.

Discussion: A review of reported cases suggests that leptomeningeal implantation may be an important step in metastases of craniopharyngioma, although the mechanism is poorly understood. Attention to tumor spillage at the time of surgery may be important in preventing distant recurrences.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00381-009-0917-4DOI Listing

Publication Analysis

Top Keywords

metastatic craniopharyngioma
8
craniopharyngioma
6
craniopharyngioma case
4
case report
4
report literature
4
literature review
4
review background
4
background distant
4
distant spread
4
spread craniopharyngioma
4

Similar Publications

Article Synopsis
  • * The girl experienced a rapid decline after surgery, ultimately resulting in life-threatening infarcts due to MMS, highlighting the need for timely diagnosis of this condition post-radiotherapy.
  • * To mitigate risks during treatment for tumor recurrence, medical management and revascularization are key, along with a recommendation for a trans-nasal surgical approach to preserve blood flow from existing collaterals.
View Article and Find Full Text PDF

Objective: Hepatopulmonary syndrome (HPS) is a rare complication of metabolic associated fatty liver disease (MAFLD) occurring subsequent to hypopituitarism, often developing after resection of hypothalamic or pituitary tumors. The aim of this study is to report an illustrative case of an HPS patient who was successfully treated with growth hormone replacement therapy, without liver transplantation which is conventionally regarded as the only treatment option. Additionally, we conducted a comprehensive review of published case reports of HPS in the pediatric population.

View Article and Find Full Text PDF
Article Synopsis
  • Adipsic arginine vasopressin deficiency (AAVP-D) occurs due to hypothalamic dysfunction, often linked to conditions like craniopharyngiomas, which makes management difficult since key mechanisms for regulating plasma osmolality are impaired.
  • Patients with AAVP-D can suffer from severe dehydration and elevated sodium levels (hypernatraemia), leading to frequent emergency visits despite treatment with desmopressin, an arginine vasopressin analogue.
  • A case study highlights the successful management of AAVP-D through careful water intake regulation and desmopressin administration, resulting in stable serum sodium levels (140-150 mmol/L) and no emergency visits over a three-month period.
View Article and Find Full Text PDF
Article Synopsis
  • - Diabetes insipidus (DI) is linked to abnormal water balance, leading to excessive urination and thirst, with Central DI often caused by factors like autoimmune issues or tumors affecting the brain.
  • - A unique case involved a 56-year-old male with small-cell lung carcinoma, initially presenting with symptoms of DI and skin swellings, but the primary lung cancer was undetected at first.
  • - Diagnostic tests, including imaging and fine needle aspiration, eventually revealed advanced lung cancer with brain metastases, confirming the link between DI symptoms and the underlying malignancy, prompting palliative care.
View Article and Find Full Text PDF
Article Synopsis
  • * There are two main types of craniopharyngioma: adamantinomatous, which is common in children and linked to mutations in the CTNNB1 gene, and papillary, which mainly affects adults and is associated with BRAF mutations.
  • * Treatment requires specialized centers to balance effective tumor removal with the preservation of critical brain function, and while surgery is essential, radiotherapy is used to minimize recurrence, alongside emerging targeted medical therapies.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!