# Bilateral extramidline involvement in intracranial germinoma: diagnostic lessons from a complex presentation

**Authors:** Fei He, Renato P. Munhoz, Suneil K. Kalia, Leah M. Skory, David F. Tang-Wai

PMC · DOI: 10.1055/s-0046-1816037 · Arquivos de Neuro-Psiquiatria · 2026-02-27

## TL;DR

A rare case of intracranial germinoma with unusual bilateral brain involvement is described, emphasizing the importance of early diagnosis for effective treatment.

## Contribution

Highlights a rare presentation of intracranial germinoma with bilateral extramidline lesions and non-specific symptoms.

## Key findings

- The patient exhibited multifocal lesions in bilateral basal ganglia, fornices, and pineal region.
- Brain biopsy confirmed intracranial germinoma despite normal tumor markers and unremarkable cerebrospinal fluid studies.

## Abstract

A 25-year-old man presented with subacute progressive anxiety, cognitive deficits, hypernatremia, and left hemiparesis. Magnetic resonance imaging demonstrated multifocal lesions in bilateral basal ganglia (globus pallidus and putamen), fornices, pineal region, along with Wallerian degeneration of the right corticospinal tract with right brainstem atrophy. Serum B-hCG, alpha-fetoprotein, alkaline phosphatase, and placental alkaline phosphatase were normal. Cerebrospinal fluid studies were unremarkable. Brain biopsy revealed intracranial germinoma. The case herein presented highlights a rare presentation of an uncommon neuro-oncological condition that often demonstrates excellent treatment response but is often diagnosed late due to its non-specific presenting symptoms.

## Linked entities

- **Diseases:** intracranial germinoma (MONDO:0002214)

## Full-text entities

- **Genes:** DNER (delta/notch like EGF repeat containing) [NCBI Gene 92737] {aka UNQ26, bet}, RCVRN (recoverin) [NCBI Gene 5957] {aka RCV1}, AQP4 (aquaporin 4) [NCBI Gene 361] {aka MIWC, MLC4, WCH4, hAQP4}, LGI1 (leucine rich glioma inactivated 1) [NCBI Gene 9211] {aka ADLTE, ADPAEF, ADPEAF, DEE121, EPITEMPIN, EPT}, KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815] {aka C-Kit, CD117, MASTC, PBT, SCFR}, SALL4 (spalt like transcription factor 4) [NCBI Gene 57167] {aka DRRS, HSAL4, IVIC, ZNF797}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, TNFRSF8 (TNF receptor superfamily member 8) [NCBI Gene 943] {aka CD30, D1S166E, Ki-1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TTN (titin) [NCBI Gene 7273] {aka CMD1G, CMH9, CMPD4, CMYO5, CMYP5, EOMFC}, PNMA2 (PNMA family member 2) [NCBI Gene 10687] {aka MA2, MM2, RGAG2}, CNTNAP2 (contactin associated protein 2) [NCBI Gene 26047] {aka AUTS15, CASPR2, CDFE, NRXN4, PTHSL1}, ZIC4 (Zic family zinc finger 4) [NCBI Gene 84107], GPC3 (glypican 3) [NCBI Gene 2719] {aka DGSX, GTR2-2, MXR7, OCI-5, SDYS, SGB}, DPP6 (dipeptidyl peptidase like 6) [NCBI Gene 1804] {aka DPL1, DPPX, MRD33, VF2}, SOX1 (SRY-box transcription factor 1) [NCBI Gene 6656], MOG (myelin oligodendrocyte glycoprotein) [NCBI Gene 4340] {aka BTN6, BTNL11, MOGIG2, NRCLP7}, BMPER (BMP binding endothelial regulator) [NCBI Gene 168667] {aka CRIM3, CV-2, CV2}, GAD2 (glutamate decarboxylase 2) [NCBI Gene 2572] {aka GAD65}
- **Diseases:** Anxiety (MESH:D001007), atrophy (MESH:D001284), asthma (MESH:D001249), hemiparesis (MESH:D010291), PRESENTATION (MESH:D001946), impairments in both frontal executive and anterograde memory functions (MESH:D020324), diabetes insipidus (MESH:D003919), malignant neoplasm (MESH:D009369), sarcoidosis (MESH:D012507), weakness (MESH:D018908), midbrain (MESH:D020295), endocrinopathy (MESH:C567425), Germinomas (MESH:D018237), irritability (MESH:D001523), hemiatrophy (MESH:D005150), syphilis (MESH:D013587), abnormalities (MESH:D000014), central diabetes insipidus (MESH:D020790), headache (MESH:D006261), globus pallidus lesion (MESH:D000079564), autoimmune or inflammatory disorder (MESH:D007249), spasticity (MESH:D009128), papilledema (MESH:D010211), disease (MESH:D004194), memory impairment (MESH:D008569), TEACHING POINTS (MESH:C000719195), brain tumors (MESH:D001932), Wallerian degeneration of corticospinal tract (MESH:C531847), Cognitive impairments (MESH:D003072), paraneoplastic (MESH:D010257), Wallerian degeneration (MESH:D014855), hypernatremia (MESH:D006955), left foot drop (MESH:D020427), central nervous system (CNS) germ cell tumours (MESH:D009373), migraine (MESH:D008881), fungal (MESH:D009181), visual field deficits (MESH:D005128), sensation deficit (MESH:D009461), LEARNED (MESH:D007859), hepatitis (MESH:D056486), ankle clonus (MESH:D016512), autoimmune (MESH:D001327), nausea (MESH:D009325), frontal-dysexecutive syndrome (MESH:D020233), degeneration (MESH:D009410)
- **Chemicals:** etoposide (MESH:D005047), cortisol (MESH:D006854), carboplatin (MESH:D016190), testosterone (MESH:D013739), H2O (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606], Canis lupus familiaris (dog, subspecies) [taxon 9615]

## Full text

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## Figures

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## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12948506/full.md

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Source: https://tomesphere.com/paper/PMC12948506