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Endoscopic endonasal management of sellar and suprasellar xanthogranulomas: A single-center experience

Yıl 2025, Cilt: 9 Sayı: 3, 432 - 438, 31.12.2025
https://doi.org/10.29058/mjwbs.1812573

Öz

Aim: Sellar xanthogranuloma (XG) is a rare, tumor-like inflammatory lesion that often mimics Rathke’s cleft cysts or craniopharyngiomas radiologically and clinically. The endoscopic endonasal approach (EEA) has become the preferred surgical corridor for these midline cystic lesions; however, evidence on optimal extent of resection and postoperative outcomes remains limited. We analyzed the clinical, radiologic, and surgical features of pathologically confirmed sellar/suprasellar XGs treated via EEA at a tertiary skull-base center.
Material and Methods: We retrospectively reviewed a prospectively maintained database of 6,597 EEAs performed between 1997 and 2025 and identified eight histologically confirmed XG cases. Demographics, presenting symptoms, imaging characteristics, surgical approach, extent of resection, and postoperative outcomes were analyzed.
Results: The cohort comprised five females and three males (median age, 26.5 years; range, 13–67). Lesions were suprasellar in five patients (62.5%) and sellar in three (37.5%). Gross-total resection was achieved in seven patients (87.5%), and subtotal resection in one (12.5%). Postoperative complications included one cerebrospinal fluid (CSF) leak after an extended suprasellar approach (12.5%) and one case of transient diabetes insipidus; no other complications were observed. No recurrences were detected during follow-up.
Conclusion: Sellar xanthogranulomas are benign inflammatory-degenerative lesions that closely resemble Rathke’s cleft cysts and craniopharyngiomas, rendering preoperative diagnosis challenging. EEA enables effective decompression with low morbidity when reconstruction is tailored to CSF-leak flow and capsule management is individualized. Long-term radiologic surveillance is preferable to aggressive reoperation.

Kaynakça

  • Lozovanu V, Georgescu CE, Florescu LM, Georgiu C, Silaghi H, Fratea A, et al. Xanthogranuloma of the Sellar Region: A Comprehensive Review of Neuroimaging in a Rare Inflammatory Entity. J Pers Med. 2022;12. https://doi.org/10.3390/jpm12060943.
  • Sprau A, Mahavadi A, Zhang M, Saste M, Deftos M, Singh H. Rathke’s cleft cyst with xanthogranulomatous change: A case report and review of the literature. Surg Neurol Int. 2020;11:246. https://doi.org/10.25259/SNI_277_2020.
  • Fujio S, Takajo T, Kinoshita Y, Hanaya R, Arimura H, Sugata J, et al. Sellar Xanthogranuloma: A Quest Based on Nine Cases Assessed with an Anterior Pituitary Provocation Test. World Neurosurg. 2019;130:e150–9. https://doi.org/10.1016/j.wneu.2019.06.021.
  • Ved R, Logier N, Leach P, Davies JS, Hayhurst C. Pituitary xanthogranulomas: clinical features, radiological appearances and post-operative outcomes. Pituitary. 2018;21:256–65. https://doi.org/10.1007/s11102-017-0859-x.
  • Fernández SC, Bernhardt MC, Grondona E, Venier AC, Bertolino ML, Pautasso MJ, et al. Sellar xanthogranuloma as a diagnostic challenge: a report on five cases. Front Neurosci. 2023;17. https://doi.org/10.3389/fnins.2023.1227144.
  • Louis DN, Perry A, Wesseling P, Brat DJ, Cree IA, Figarella-Branger D, et al. The 2021 WHO Classification of Tumors of the Central Nervous System: a summary. Neuro Oncol. 2021;23:1231–51. https://doi.org/10.1093/neuonc/noab106.
  • Nishiuchi T, Murao K, Imachi H, Kushida Y, Haba R, Kawai N, et al. Xanthogranuloma of the intrasellar region presenting in pituitary dysfunction: a case report. J Med Case Rep. 2012;6:119. https://doi.org/10.1186/1752-1947-6-119.
  • Zhang X, Yang J, Huang Y, Liu Y, Chen L, Chen F, et al. Endoscopic Endonasal Resection of Symptomatic Rathke Cleft Cysts: Total Resection or Partial Resection. Front Neurol. 2021;12:701177. https://doi.org/10.3389/fneur.2021.701177.
  • Li G, Zhang C, Sun Y, Mu Q, Huang H. Xanthogranulomatous pituitary adenoma: A case report and literature review. Mol Clin Oncol. 2018:8;445-448. https://doi.org/10.3892/mco.2018.1547.
  • Kleinschmidt‐DeMasters BK, Lillehei KO, Hankinson TC. Review of xanthomatous lesions of the sella. Brain Pathology. 2017;27:377–395. https://doi.org/10.1111/bpa.12498.
  • Rahmani R, Sukumaran M, Donaldson AM, Akselrod O, Lavi E, Schwartz TH. Parasellar xanthogranulomas. J Neurosurg. 2015;122:812–817. https://doi.org/10.3171/2014.12.JNS14542.
  • Paulus W, Honegger J, Keyvani K, Fahlbusch R. Xanthogranuloma of the sellar region: a clinicopathological entity different from adamantinomatous craniopharyngioma. Acta Neuropathol. 1999;97:377–382. https://doi.org/10.1007/s004010051001.
  • Nishioka H, Shibuya M, Ohtsuka K, Ikeda Y, Haraoka J. Endocrinological and MRI features of pituitary adenomas with marked xanthogranulomatous reaction. Neuroradiology. 2010;52:997–1002. https://doi.org/10.1007/s00234-010-0675-8.
  • Neubauer C, Shah M, Meckel S. Selläres Xanthogranulom: MRT-Bildgebung und Differenzialdiagnose. RöFo - Fortschritte Auf Dem Gebiet Der Röntgenstrahlen Und Der Bildgebenden Verfahren. 2012;185:272–274. https://doi.org/10.1055/s-0032-1325514.
  • Alharbi A, Alkhaibary A, Alaglan A, Khairy S, Alkhunaizi Z, AlSufiani F, et al. Sellar xanthogranuloma: A diagnostic challenge. Surg Neurol Int. 2022;13:76. https://doi.org/10.25259/SNI_1180_2021.
  • Madan Mohan B, Mohamed E, Jain SK, Jain M, Jaiswal AK. Serial MR Imaging in Suprasellar Xanthogranuloma: Growth Pattern and New Lesions. Journal of Neuroimaging. 2015;25:677–679. https://doi.org/10.1111/jon.12170.
  • Nishiuchi T, Murao K, Imachi H, Kushida Y, Haba R, Kawai N, et al. Xanthogranuloma of the intrasellar region presenting in pituitary dysfunction: a case report. J Med Case Rep. 2012;6:119. https://doi.org/10.1186/1752-1947-6-119.
  • Kunii N, Abe T, Kawamo M, Tanioka D, Izumiyama H, Moritani T. Rathke’s cleft cysts: differentiation from other cystic lesions in the pituitary fossa by use of single-shot fast spin-echo diffusion-weighted MR imaging. Acta Neurochir (Wien). 2007;149:759–769. https://doi.org/10.1007/s00701-007-1234-x.
  • Ved R, Logier N, Leach P, Davies JS, Hayhurst C. Pituitary xanthogranulomas: clinical features, radiological appearances and post-operative outcomes. Pituitary. 2018;21:256–265. https://doi.org/10.1007/s11102-017-0859-x.
  • Agarwal A, Agarwal K, Lee HK. Xanthogranuloma of the Sellar Region. Neuroradiol J. 2012;25:181–184. https://doi.org/10.1177/197140091202500204.
  • Prieto R, Pascual JM. Craniopharyngiomas with a mixed histological pattern: the missing link to the intriguing pathogenesis of adamantinomatous and squamous‐papillary varieties? Neuropathology. 2013;33:682–686. https://doi.org/10.1111/neup.12030.
  • Yang B, Yang C, Fang J, Li G, Wang J, Jia G, et al. Clinicoradiologic Features and Surgical Outcomes of Sellar Xanthogranulomas: A Single-Center 10-Year Experience. World Neurosurg. 2017;99:439–447. https://doi.org/10.1016/j.wneu.2016.12.017.
  • Lozovanu V, Georgescu CE, Florescu LM, Georgiu C, Silaghi H, Fratea A, et al. Xanthogranuloma of the Sellar Region: A Comprehensive Review of Neuroimaging in a Rare Inflammatory Entity. J Pers Med. 2022;12:943. https://doi.org/10.3390/jpm12060943.
  • Guerrero-Pérez F, Marengo AP, Vilarrasa N, Vidal N, Ruiz-Roig N, Sánchez-Fernández JJ, et al. Xanthogranuloma of the sellar region: a systematic review. Hormones. 2023;22:199–210. https://doi.org/10.1007/s42000-023-00432-y.
  • Topaloğlu Ö, Açıkgöz GG, Tekin S, Malkoç B, Kaymaz E, Karadeniz Çakmak G, et al. Difficulty in Follow-Up of Papillary Thyroid Cancer Co-Existent with Hypopituitarism: Case Report and Review of the Literature. Med J West Black Sea. 2022;6(3):410-416. https://doi.org/10.29058/mjwbs.1164665

Sellar ve suprasellar ksantogranülomaların endoskopik endonazal yönetimi: Tek merkez deneyimi

Yıl 2025, Cilt: 9 Sayı: 3, 432 - 438, 31.12.2025
https://doi.org/10.29058/mjwbs.1812573

Öz

Amaç: Sellar ksantogranüloma (XG), radyolojik ve klinik olarak sıklıkla Rathke yarığı kistleri veya kraniofaringiomlarla karışan, nadir görülen, tümör benzeri inflamatuvar bir lezyondur. Endoskopik endonazal yaklaşım (EEA), bu orta hat kistik lezyonları için tercih edilen cerrahi yol haline gelmiştir; ancak optimal rezeksiyon düzeyi ve ameliyat sonrası sonuçlara ilişkin veriler sınırlıdır. Bu çalışmada, üçüncü basamak bir kafa tabanı merkezinde endoskopik endonazal yaklaşımla tedavi edilen patolojik olarak doğrulanmış sellar ve suprasellar ksantogranülomaların klinik, radyolojik ve cerrahi özellikleri analiz edilmiştir.
Gereç ve Yöntemler: 1997–2025 yılları arasında gerçekleştirilen 6.597 endoskopik endonazal cerrahi içeren prospektif olarak tutulan bir veri tabanının retrospektif incelemesi sonucunda, histolojik olarak doğrulanmış sekiz ksantogranüloma olgusu belirlenmiştir. Demografik veriler, başvuru semptomları, görüntüleme bulguları, cerrahi yaklaşım, rezeksiyon düzeyi ve ameliyat sonrası sonuçlar analiz edilmiştir.
Bulgular: Kohortta beş kadın ve üç erkek hasta yer almakta olup, ortanca yaş 26,5 (dağılım 13–67) idi. Lezyonlar beş hastada (%62,5) suprasellar, üç hastada (%37,5) sellar yerleşimliydi. Yedi hastada (%87,5) total rezeksiyon, bir hastada (%12,5) subtotal rezeksiyon gerçekleştirildi. Bir hastada (%12,5) genişletilmiş suprasellar yaklaşımdan sonra ameliyat sonrası beyin omurilik sıvısı (BOS) kaçağı, bir diğer hastada ise geçici diabetes insipidus gelişti; başka komplikasyon gözlenmedi. Takip süresince nüks saptanmadı.
Sonuç: Sellar ksantogranülomalar, Rathke yarığı kistleri ve kraniofaringiomlarla benzer özellikler gösteren, benign inflamatuvar-dejeneratif lezyonlardır ve bu nedenle preoperatif tanı sıklıkla güçtür. Endoskopik endonazal cerrahi, BOS kaçağı derecesine göre uyarlanmış rekonstrüksiyon ve bireyselleştirilmiş kapsül yönetimi ile düşük morbiditeyle etkili bir dekompresyon sağlar. Uzun dönem radyolojik izlem, agresif yeniden cerrahiye tercih edilmelidir.

Kaynakça

  • Lozovanu V, Georgescu CE, Florescu LM, Georgiu C, Silaghi H, Fratea A, et al. Xanthogranuloma of the Sellar Region: A Comprehensive Review of Neuroimaging in a Rare Inflammatory Entity. J Pers Med. 2022;12. https://doi.org/10.3390/jpm12060943.
  • Sprau A, Mahavadi A, Zhang M, Saste M, Deftos M, Singh H. Rathke’s cleft cyst with xanthogranulomatous change: A case report and review of the literature. Surg Neurol Int. 2020;11:246. https://doi.org/10.25259/SNI_277_2020.
  • Fujio S, Takajo T, Kinoshita Y, Hanaya R, Arimura H, Sugata J, et al. Sellar Xanthogranuloma: A Quest Based on Nine Cases Assessed with an Anterior Pituitary Provocation Test. World Neurosurg. 2019;130:e150–9. https://doi.org/10.1016/j.wneu.2019.06.021.
  • Ved R, Logier N, Leach P, Davies JS, Hayhurst C. Pituitary xanthogranulomas: clinical features, radiological appearances and post-operative outcomes. Pituitary. 2018;21:256–65. https://doi.org/10.1007/s11102-017-0859-x.
  • Fernández SC, Bernhardt MC, Grondona E, Venier AC, Bertolino ML, Pautasso MJ, et al. Sellar xanthogranuloma as a diagnostic challenge: a report on five cases. Front Neurosci. 2023;17. https://doi.org/10.3389/fnins.2023.1227144.
  • Louis DN, Perry A, Wesseling P, Brat DJ, Cree IA, Figarella-Branger D, et al. The 2021 WHO Classification of Tumors of the Central Nervous System: a summary. Neuro Oncol. 2021;23:1231–51. https://doi.org/10.1093/neuonc/noab106.
  • Nishiuchi T, Murao K, Imachi H, Kushida Y, Haba R, Kawai N, et al. Xanthogranuloma of the intrasellar region presenting in pituitary dysfunction: a case report. J Med Case Rep. 2012;6:119. https://doi.org/10.1186/1752-1947-6-119.
  • Zhang X, Yang J, Huang Y, Liu Y, Chen L, Chen F, et al. Endoscopic Endonasal Resection of Symptomatic Rathke Cleft Cysts: Total Resection or Partial Resection. Front Neurol. 2021;12:701177. https://doi.org/10.3389/fneur.2021.701177.
  • Li G, Zhang C, Sun Y, Mu Q, Huang H. Xanthogranulomatous pituitary adenoma: A case report and literature review. Mol Clin Oncol. 2018:8;445-448. https://doi.org/10.3892/mco.2018.1547.
  • Kleinschmidt‐DeMasters BK, Lillehei KO, Hankinson TC. Review of xanthomatous lesions of the sella. Brain Pathology. 2017;27:377–395. https://doi.org/10.1111/bpa.12498.
  • Rahmani R, Sukumaran M, Donaldson AM, Akselrod O, Lavi E, Schwartz TH. Parasellar xanthogranulomas. J Neurosurg. 2015;122:812–817. https://doi.org/10.3171/2014.12.JNS14542.
  • Paulus W, Honegger J, Keyvani K, Fahlbusch R. Xanthogranuloma of the sellar region: a clinicopathological entity different from adamantinomatous craniopharyngioma. Acta Neuropathol. 1999;97:377–382. https://doi.org/10.1007/s004010051001.
  • Nishioka H, Shibuya M, Ohtsuka K, Ikeda Y, Haraoka J. Endocrinological and MRI features of pituitary adenomas with marked xanthogranulomatous reaction. Neuroradiology. 2010;52:997–1002. https://doi.org/10.1007/s00234-010-0675-8.
  • Neubauer C, Shah M, Meckel S. Selläres Xanthogranulom: MRT-Bildgebung und Differenzialdiagnose. RöFo - Fortschritte Auf Dem Gebiet Der Röntgenstrahlen Und Der Bildgebenden Verfahren. 2012;185:272–274. https://doi.org/10.1055/s-0032-1325514.
  • Alharbi A, Alkhaibary A, Alaglan A, Khairy S, Alkhunaizi Z, AlSufiani F, et al. Sellar xanthogranuloma: A diagnostic challenge. Surg Neurol Int. 2022;13:76. https://doi.org/10.25259/SNI_1180_2021.
  • Madan Mohan B, Mohamed E, Jain SK, Jain M, Jaiswal AK. Serial MR Imaging in Suprasellar Xanthogranuloma: Growth Pattern and New Lesions. Journal of Neuroimaging. 2015;25:677–679. https://doi.org/10.1111/jon.12170.
  • Nishiuchi T, Murao K, Imachi H, Kushida Y, Haba R, Kawai N, et al. Xanthogranuloma of the intrasellar region presenting in pituitary dysfunction: a case report. J Med Case Rep. 2012;6:119. https://doi.org/10.1186/1752-1947-6-119.
  • Kunii N, Abe T, Kawamo M, Tanioka D, Izumiyama H, Moritani T. Rathke’s cleft cysts: differentiation from other cystic lesions in the pituitary fossa by use of single-shot fast spin-echo diffusion-weighted MR imaging. Acta Neurochir (Wien). 2007;149:759–769. https://doi.org/10.1007/s00701-007-1234-x.
  • Ved R, Logier N, Leach P, Davies JS, Hayhurst C. Pituitary xanthogranulomas: clinical features, radiological appearances and post-operative outcomes. Pituitary. 2018;21:256–265. https://doi.org/10.1007/s11102-017-0859-x.
  • Agarwal A, Agarwal K, Lee HK. Xanthogranuloma of the Sellar Region. Neuroradiol J. 2012;25:181–184. https://doi.org/10.1177/197140091202500204.
  • Prieto R, Pascual JM. Craniopharyngiomas with a mixed histological pattern: the missing link to the intriguing pathogenesis of adamantinomatous and squamous‐papillary varieties? Neuropathology. 2013;33:682–686. https://doi.org/10.1111/neup.12030.
  • Yang B, Yang C, Fang J, Li G, Wang J, Jia G, et al. Clinicoradiologic Features and Surgical Outcomes of Sellar Xanthogranulomas: A Single-Center 10-Year Experience. World Neurosurg. 2017;99:439–447. https://doi.org/10.1016/j.wneu.2016.12.017.
  • Lozovanu V, Georgescu CE, Florescu LM, Georgiu C, Silaghi H, Fratea A, et al. Xanthogranuloma of the Sellar Region: A Comprehensive Review of Neuroimaging in a Rare Inflammatory Entity. J Pers Med. 2022;12:943. https://doi.org/10.3390/jpm12060943.
  • Guerrero-Pérez F, Marengo AP, Vilarrasa N, Vidal N, Ruiz-Roig N, Sánchez-Fernández JJ, et al. Xanthogranuloma of the sellar region: a systematic review. Hormones. 2023;22:199–210. https://doi.org/10.1007/s42000-023-00432-y.
  • Topaloğlu Ö, Açıkgöz GG, Tekin S, Malkoç B, Kaymaz E, Karadeniz Çakmak G, et al. Difficulty in Follow-Up of Papillary Thyroid Cancer Co-Existent with Hypopituitarism: Case Report and Review of the Literature. Med J West Black Sea. 2022;6(3):410-416. https://doi.org/10.29058/mjwbs.1164665
Toplam 25 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Beyin ve Sinir Cerrahisi (Nöroşirurji)
Bölüm Araştırma Makalesi
Yazarlar

Atakan Emengen 0000-0002-6853-1540

Eren Yılmaz 0000-0002-5911-7268

Ayşe Uzuner 0000-0002-6471-7452

Aykut Gökbel 0000-0002-9332-3321

Savaş Ceylan 0000-0002-2747-8907

Gönderilme Tarihi 29 Ekim 2025
Kabul Tarihi 25 Kasım 2025
Yayımlanma Tarihi 31 Aralık 2025
Yayımlandığı Sayı Yıl 2025 Cilt: 9 Sayı: 3

Kaynak Göster

Vancouver 1.Emengen A, Yılmaz E, Uzuner A, Gökbel A, Ceylan S. Endoscopic endonasal management of sellar and suprasellar xanthogranulomas: A single-center experience. Med J West Black Sea [Internet]. 01 Aralık 2025;9(3):432-8. Erişim adresi: https://izlik.org/JA92CB66YG

Batı Karadeniz Tıp Dergisi, Zonguldak Bülent Ecevit Üniversitesi tarafından yayımlanan, uluslararası, hakemli ve açık erişimli bir dergidir. İlk sayısı 2017 yılında yayımlanan dergi, yılda üç kez (Nisan, Ağustos ve Aralık aylarında) yayımlanmakta olup Türkçe ve İngilizce makalelere yer verir.