| Naslov: | Two illustrative cases of adult Lhermitte-Duclos disease and a systematic review of literature related to surgical management |
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| Avtorji: | ID Lakicevic, Goran (Avtor)
ID Tinjak-Demic, Selma (Avtor)
ID Lakicevic, Sandra (Avtor)
ID Frol, Senta (Avtor)
ID Splavski, Bruno (Avtor) |
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| Datoteke: |  PDF - Predstavitvena datoteka, prenos (4,95 MB)
MD5: F2BDB0497327F30F273A614925F1460F
 URL - Izvorni URL, za dostop obiščite https://www.sciencedirect.com/science/article/pii/S2772529425000773
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| Jezik: | Angleški jezik |
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| Tipologija: | 1.01 - Izvirni znanstveni članek |
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| Organizacija: |  UKC LJ - Univerzitetni klinični center Ljubljana
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| Povzetek: | Background Lhermitte-Duclos disease is a rare subtype of gangliocytoma, a benign tumor growth in the cerebellum often associated with Cowden syndrome, a sporadic genetic pleomorphic disorder that is inherited in an autosomal dominant manner and caused by a harmful mutation in the PTEN gene. Such a mutation can originate malignant and benign tumors, including dysplastic gangliocytoma of the posterior cranial fossa. Methods We present two illustrative cases of Lhermitte-Duclos disease that we encountered and surgically treated during the last few years. We also performed a systematic literature review concerned with the surgical management of Lhermitte-Duclos disease and Cowden syndrome. Results Both patients were young females complaining of occipital headaches and underwent brain MRIs that revealed unilateral discrete cerebellar atrophy and expansive lesions of the posterior cranial fossa with characteristic striate T-2 weighted hyperintensity resembling tiger fur. They were both successfully operated on due to the posterior fossa dysplastic gangliocytoma, which was histopathologically confirmed as Lhermitte-Duclos disease. In one patient, genetic testing confirmed a PTEN mutation characteristic for Cowden syndrome. Conclusion Early diagnosis, genetic testing, and close monitoring are obligatory to enhance the knowledge of Lhermitte-Duclos disease and its probable association with Cowden syndrome to decrease the risk of malignancy of other organs and organic systems. Surgical posterior fossa decompression is required at the onset of neurological symptoms to relieve the mass effect and provide tissue samples for further analysis, ensuring a favorable outcome. |
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| Ključne besede: | cases, Lhermitte-Duclos, nevrokirurgija |
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| Status publikacije: | Objavljeno |
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| Verzija publikacije: | Objavljena publikacija |
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| Leto izida: | 2025 |
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| Št. strani: | 6 str. |
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| Številčenje: | Vol. 5, [article no.] ǂ104258 |
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| PID: | 20.500.12556/DiRROS-28051  |
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| UDK: | 616.8-089 |
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| ISSN pri članku: | 2772-5294 |
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| DOI: | 10.1016/j.bas.2025.104258 |
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| COBISS.SI-ID: | 237481987 |
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| Opomba: | Nasl. z nasl. zaslona;
Opis vira z dne 28. 5. 2025;
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| Datum objave v DiRROS: | 09.03.2026 |
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| Število ogledov: | 267 |
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| Število prenosov: | 172 |
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| Metapodatki: |    |
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