Case Report - (2023) Volume 13, Issue 5
Received: 26-Feb-2020, Manuscript No. JCCR-23-7742;
Editor assigned: 02-Mar-2020, Pre QC No. PreQC No. P-7742;
Reviewed: 16-Mar-2020, QC No. QC No. Q-7742;
Revised: 19-Jul-2023, Manuscript No. R-7742;
Published:
16-Aug-2023
, DOI: 10.37421/2165-7920.2023.13.1579
, QI Number: JCCR-23-7742
Citation: Nishimura, Fumihiko, Miho Kakutani, Young-
Soo Park and Yasushi Motoyama, et al.. "A Case of
Craniopharyngioma with Malignant Transformation after not Radiation Therapy
but Growth Hormone Replacement Therapy." J Clin Case Rep 13 (2023):
1572.
Copyright: © 2023 Nishimura F, et al. This is an open-access article distributed under the terms of the creative commons attribution license which permits
unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
Background: We present a rare case of malignant transformation of a craniopharyngioma in a patient who received growth hormone replacement therapy.
Case description: A 43-year-old male came to our department with a headache and visual disturbance and was admitted. Brain Magnetic Resonance Imaging (MRI) revealed a giant tumor in the intra- and suprasellar region compressing the optic chiasma. Using a transcranial pterional approach the tumor removal was performed as much as possible with the residual mass removed later with a trans-sphenoidal approach. The initial histopathological diagnosis was adamantinomatous craniopharyngioma. Decompression of the optic chiasma was achieved and visual function improved though residual tumor tissue remained in the parasellar region without regrowth seen for more than 24 years. At the age of 67 years the patient received growth hormone replacement therapy because of a deficiency then 2 years later the residual tumor began to gradually grow. Trans-sphenoidal surgery was again performed to remove the growing tumor and histopathology results revealed an adamantinomatous craniopharyngioma with malignant transformation. Stereotactic radiation therapy was performed for the residual mass with a total dose of 60 Gy. Presently 1 year later the patient has a stable condition and the tumor remains controlled while follow-up examinations are continuing.
Conclusion: A craniopharyngioma may undergo malignant transformation with continuous exposure to administered growth hormone. Close follow-up and imaging examinations are necessary to detect a change including tumor growth in such cases.
Malignant transformation • Craniopharyngioma • Growth hormone • Radiation therapy
WHO: World Health Organization; SRT: Stereotactic Radiotherapy; GH: Growth Hormone; Gd: Gadolinium; Gy: Gray; MRI: Magnetic Resonance Imaging; CT: Computed Tomography
A craniopharyngioma which originates from Rathke’s pouch a derivative of the oral ectoderm is a benign tumor that accounts for approximately 3%-3.5% of all intracranial tumors. Recurrence following a total resection procedure has been reported to occur in 30% of such cases while that after subtotal resection occurs in 50%-70% thus adjuvant radiotherapy following a subtotal procedure has been recommended [1-3].
Malignant transformation of a craniopharyngioma rarely occurs and the etiology and pathogenesis of those cases are unclear though a previous study suggested a correlation with radiotherapy. There are no known reports of a case with malignant transformation associated with Growth Hormone (GH) replacement therapy. The prognosis of individuals with a malignantly transformed craniopharyngioma is considered to be poor though the incidence rate is low and there is insufficient evidence regarding available treatment modalities. Herein we present a case of craniopharyngioma with subsequent malignant transformation that occurred 2 years after GH replacement therapy without radiotherapy [4].
A 43-year-old male came to our department in 1992 with a headache and visual disturbance and was admitted. Brain Magnetic Resonance Imaging (MRI) revealed a tumor in the intra- and suprasellar region compressing the optic chiasma. Using a transcranial pterional approach tumor removal was performed with the residual mass removed later with a trans-sphenoidal approach. The histopathological diagnosis was typical adamantinomatous craniopharyngioma (Figure 1). There was no cytologic atypia or mitosis. Decompression of the optic chiasma was achieved and visual function improved though residual tumor tissue remained around the parasellar region (Figure 2). Thereafter the residual tumor did not show regrowth for more than 24 years [5,6].
Figure 1. The histopathologic diagnosis was adamantinomatous craniopharyngioma. There were no findings of cytologic atypia or mitosis. Hematoxylin-eosin staining (original magnification × 200).
Figure 2. Results of brain MRI with Gd following transcranial and trans-sphenoidal surgery. Following those procedures residual tumor tissue remained around the parasellar region. A) Coronal section; B) Sagittal section.
In 2016 severe GH deficiency was noted and the patient underwent GH replacement therapy at the age of 67. However 2 years later the residual tumor began to grow (Figure 3). Thus transsphenoidal surgery was again performed to remove the growing tumor (Figures 4 and 5). Histopathological results revealed an adamantinomatous craniopharyngioma with cytologically malignant features (Figure 5A) [7]. The tumor cells showed significant nuclear pleomorphism hyperchromasia and a high nuclear-cytoplasmic ratio indicating malignant transformation (Figure 5B). Furthermore immunohistochemistry findings showed a Ki67 proliferation rate 45% and overexpression of p53 (Figure 5C and 5D). To prevent growth of the residual tumor adjuvant stereotactic radiotherapy was performed with a total dose of 60 Gy in 30 fractions (Figure 6). Presently, 1 year after radiotherapy the patient is in stable condition and the tumor is controlled [8].
Figure 3. Results of brain MRI with Gd at 2 years after starting growth hormone therapy. The tumor showed aggressive growth. A) Coronal section; B) Sagittal section.
Figure 4. Results of brain MRI with Gd after trans-sphenoidal surgery. A) Coronal section; B) Sagittal section.
Figure 5. Histopathology findings revealed malignant transformation of the craniopharyngioma. A) Hematoxylin-eosin stain (original magnification × 200); B) Tumor cells showed significant nuclear pleomorphism (white arrows) hematoxylineosin stain (original magnification × 200); C) Immunohistochemistry for Ki67 (original magnification × 200); D) Immunohistochemistry for p53 (original magnification × 100).
Figure 6. Stereotactic radiotherapy dose planning (total dose 60 Gy in 30 fractions).
The World Health Organization (WHO) classifies a craniopharyngioma as a benign grade 1 tumor known for high recurrence and local aggressiveness despite treatment. However, cases with malignant transformation are extremely rare, with the first presented in 1987, 1986 for a total of 28 reported cases, of which only 6 noted a malignant craniopharyngioma without radiotherapy. Although the exact cause and pathogenesis of such malignant transformation are unknown, previous studies have speculated a likely correlation with radiotherapy. On the other hand, in a review by Sofela AA et al, there was a poor correlation found between malignant transformation and radiotherapy. The present case also showed transformation to malignancy without radiotherapy, thus we consider that there are other factors contributing to malignant transformation of a craniopharyngioma [9].
Human GH is a classical pituitary endocrine hormone essential for normal postnatal growth that has pleiotropic effects across multiple physiological systems, while its overproduction has been linked to cancer. The hormone is also expressed in extra-pituitary tissues and shows localized autocrine/paracrine effects at those sites. Although the theoretical concern of increased tumor growth for patients taking GH has been addressed by numerous studies, a meta-analysis by Shen et al, included studies and actually found that GH was associated with a decreased risk of craniopharyngioma recurrence in adults [10].
The present patient received GH replacement therapy to compensate for severe deficiency at 24 years after undergoing craniopharyngioma removal with no radiotherapy performed for the residual tumor and gradual tumor growth was noted after GH administration. Although the precise cause of progression is unknown, GH might have been a factor in the present case of malignant transformation, thus careful attention should be paid for rapid tumor growth in patients with a residual tumor who undergo GH replacement therapy [11].
Once the tumor shows transformation to malignancy, it can continue to grow even if GH replacement therapy is stopped, with tumor mass removal necessary to confirm the histopathology for determining adjuvant therapy. Continuous hormone exposure associated with GH replacement therapy may lead to malignant transformation of a craniopharyngioma. Close attention to follow-up imaging findings is necessary to detect change or rapid tumor growth following exposure to GH.
The authors declare that the contents of this article were composed in the absence of any commercial or financial relationships that could be construed as potential conflicts of interest. This research did not receive any specific grant from a funding agency in the public, commercial or not-for-profit sector.
[Google Scholar] [PubMed]
[Crossref] [Google Scholar] [PubMed]
[Google Scholar] [PubMed]
[Crossref] [Google Scholar] [PubMed]
[Crossref] [Google Scholar] [PubMed]
[Crossref] [Google Scholar] [PubMed]
[Crossref] [Google Scholar] [PubMed]
[Crossref] [Google Scholar] [PubMed]
[Crossref] [Google Scholar] [PubMed]
[Crossref] [Google Scholar] [PubMed]
Journal of Clinical Case Reports received 1345 citations as per Google Scholar report
