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Литература:

1. Samik Hazra, Saugata Acharyya, Kakoli Acharyya Primary pituitary abscess in an adolescent boy: a rare occurrence Hazra S, et al. BMJ Case Reports 2012. doi:10.1136/bcr-2012–007134

2. Hanel RA, Koerbel A, Prevedello DM, Moro MS, Araújo JC. Primary pituitary abscess: case report. Arq Neuropsiquiatr. 2002 Sep;60 (3-B):861–65. http://dx.doi. org/10.1590/S0004-282X2002000500033

3. Karagiannis AK, Dimitropoulou F, Papatheodorou A, Lyra S, Seretis A, Vryonidou A. Pituitary abscess: a case report and review of the literature. Endocrinol Diabetes Metab Case Rep. 2016;2016:160014. doi: 10.1530/EDM-16–0014

4. Giovanni Muscas, Francesco Iacoangeli, Laura Li ppa, Biagio R. Carangelo. Spontaneous rupture of a secondary pituitary abscess causing acute meningoencephalitis: Case report and literature review. Surg Neurol Int. 2017;8:177. doi: 10.4103/sni.sni_131_17

5. Agyei JO, Lipinski LJ, Leonardo J. Case Report of a Primary Pituitary Abscess and Systematic Literature Review of Pituitary Abscess with a Focus on Patient Outcomes. World Neurosurg 2017;101:76 92.

6. Jain KC, Varma A, Mahapatra AK. Pituitary abscess: a series of six cases. Br J Neurosurg 1997;11:139–43.3

7. Kotil K, Bilge T. Primary pituitary abscess mimicking an adenoma: a rare entity. Turk J Endocrinol Metab 2004;3:125–7.

8. Blackett PR, Bailey JD, Hoffman HJ. A pituitary abscess simulating an intrasellar tumor. Surg Neurol 1980;14:129–31.5

9. Kaur A, Agrawal A, Mittal M. Presumed pituitary abscess without infectious source treated successfully with antibiotics alone. J Neuroophthalmol 2005;25:185–8.

10. Takahashi T, Shibata S, Ito K, et al. Neuroimaging appearance of pituitary abscess complicated with close inflammatory lesions-case report. Neurol Med Chir (Tokyo) 1998;38:51–4.7

11. Nishimura K, Takao T, Mimoto T, et al. A case of anterior hypopituitarism showing recurrent pituitary mass associated with central diabetes insipidus. Endocr J 2003;50:825–9

12. Kim HC, Kang SG, Huh PW, Yoo do S, Cho KS, Kim DS. Pituitary abscess in a pregnant woman. J Clin Neurosci. 2007 Nov;14 (11):1135–39. doi: 10.1016/j.jocn.2006.03.012

13. Danilowicz K, Sanz CF, Manavela M, Gomez RM, Bruno OD. Pituitary abscess: a report of two cases. Pituitary. 2008;11 (1):89–92. doi: 10.1007/s11102-007-0033-y

14. Kuge A, Sato S, Takemura S, Sakurada K, Kondo R, Kayama T. Abscess formation associated with pituitary adenoma: a case report: Changes in the MRI appearance of pituitary adenoma before and after abscess formation. Surg Neurol Int. 2011 Jan 24;2:3. doi: 10.4103/2152–7806.76140

15. Meftah A, Moumen A, Eljadi H, Guerboub AA, Elmoussaoui S, Belmejdoub G. Pituitary abscess simulating a pituitary adenoma. Presse Med. 2016 Jun;45 (6 Pt 1):602–4. doi: 10.1016/j.lpm.2016.03.016 [Article in French]

16. Takayasu T, Yamasaki F, Tominaga A, Hidaka T, Arita K, Kurisu K. A pituitary abscess showing high signal intensity on diffusion-weighted imaging. Neurosurg Rev. 2006 Jul;29 (3):246–48. doi: 10.1007/s10143-006-0021-0

17. Schwartz ID, Zalles MC, Foster JL, Burry VF (1995) Pituitary abscess: an unusual presentation of ‘‘aseptic meningitis’’. J Pediatr Endocrinol Metab 8 (2):141–146

18. Carmen Emanuela Pepene 1, Ioana Ilie, Dan Mihu, Horaţiu Stan, Silviu Albu, Ileana Duncea Primary pituitary abscess followed by empty sella syndrome in an adolescent girl. 2010 Dec;13 (4):385–9. doi: 10.1007/s11102-008-0150-2

19. Zhang X, Sun J, Shen M, Shou X, Qiu H, Qiao N, Zhang N, Li S, Wang Y, Zhao Y. Diagnosis and minimally invasive surgery for the pituitary abscess: a review of twenty nine cases. Clin Neurol Neurosurg. 2012 Sep;114 (7):957–61. doi: 10.1016/j.clineuro.2012.02.020

20. Lu Gao, Xiaopeng Guo, Rui Tian, Qiang Wang1, Ming Feng, Xinjie Bao, Kan Deng, Yong Yao, Wei Lian, Renzhi Wang, Bing Xing, Pituitary abscess: clinical manifestations, diagnosis and treatment of 66 cases from a large pituitary center over 23 years. (2017) 20:189–194 DOI 10.1007/s11102-016-0757-7

21. Blackett PR, Bailey JD, Hoffman HJ. A pituitary abscess simulating an intrasellar tumor. Surg Neurol. 1980;14:129–131.

22. Dutta P, Bhansali A, Singh P, Bhat MH. Suprasellar tubercular abscess presenting as panhypopituitarism: a common lesion in an uncommon site with a brief review of literature. Pituitary. 2006;9:73–77

23. Dutta P, Bhansali A, Singh P, Kotwal N, Pathak A, Kumar Y. Pituitary abscess: report of four cases and review of literature. Pituitary. 2006;9:267–273.

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25. Jain KC, Varma A, Mahapatra AK. Pituitary abscess: a series of six cases. Br J Neurosurg. 1997;11: 139–143.

26. Kaur A, Agrawal A, Mittal M. Presumed pituitary abscess without infectious source treated successfully with antibiotics alone. J Neuroophthalmol. 2005;25:185–188.

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29. Liu F, Li G, Yao Y, Yang Y, Ma W, Li Y, et al. Diagnosis and management of pituitary abscess: experiences from 33 cases. Clin Endocrinol (Oxf ). 2011;74:79–88.

30. Bossard D, Himed A, Badet C, Lapras V, Mornex R, Fisher G, et al. MRI and CT in a case of pituitary abscess. J Neuroradiol. 1992;19: 139–144.

31. Schwartz ID, Zalles MC, Foster JL, Burry VF. Pituitary abscess: an unusual presentation of «aseptic meningitis». J Pediatr Endocrinol Metab. 1995;8:141–146.

32. Shono T, Nishio S, Muratani H, Yasuda T, Fukui M, Moutai K. Pituitary abscess secondary to isolated sphenoid sinusitis. Minim Invasive Neurosurg. 1999;42:204–206.

33. Shuster A, Gunnarsson T, Sommer D, Miller E. Pituitary abscess: an unexpected diagnosis. Pediatr Radiol. 2010;40:219–222.

34. Uchiyama T, Sakai K, Asanuma M, Aoyama T, Hongo K. Pituitary abscess manifesting as meningitis and photophobia associated with Rathke’s cleft cyst in a child. Case report. Neurol Med Chir (Tokyo). 2011;51:455– 459.

35. Vates GE, Berger MS, Wilson CB. Diagnosis and management of pituitary abscess: a review of twenty-four cases. J Neurosurg. 2001;95:233–241.

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37. P. L. Kalinin, M. A. Kutin, D. V. Fomichev, B. A. Kadashev, A. N. Shkarubo, L. I. Astafieva, Iu. G. Sidneva, O. I. Sharipov, G. E. Chmutin, D. N. Andreev, I. A. Voronina, I. V. Chernev, A. A. Abdilatipov Khururgicheskoe lechenie adenom gipofiza: uchebnoe posobiia [Surgical treatment of pituitary adenomas: Guidelines]. Moscow: RUDN, 226 p.: ISBN 978-5-209-09995-6. (In Russ.)

38. P. L. Kalinin, D. V. Fomichev, M. A. Kutin Endoskopicheskaia transsfenoidalnaia khirurgiia [Endoscopic transsphenoidal surgery], 2017, 184 p. ISBN 978-5-900758-92-3. (In Russ.)

Pituitary abscess (PA) is an acute purulent-inflammatory disease with a high risk of lethal outcome [1, 2, 3]. It was first described by Heslop in 1848 and

M. Simmonds in 1914 (cited in R. A. Hanel et al., 2002 [2]). To date, more than 200 clinical cases of this disease have been described in the world literature. This pathology is presented in publications mainly as isolated cases. PA was rarely accompanied by the development of purulent meningoencephalitis according to published cases [4]. The rare occurrence of PAH makes it difficult to determine the epidemiology of the disease, but it is thought to account for 0.2–1.1 % of all chiasmo-sellar masses — (CSR) [5,6,7].

In children, pituitary abscess is exceptionally rare. Currently, we were able to find 22 publications of primary pituitary abscess in children in the international literature. Most PAs were caused by infection from the Rathke’s pocket cleft cyst. In only a few cases, PAs had a primary pituitary origin [5, 8, 9]. Clinical diagnosis is difficult because there are no specific clinical symptoms or signs of the disease. PA often cannot be distinguished radiologically from other pituitary gland lesions. At disease manifestation, laboratory markers of inflammation (such as increased erythrocyte sedimentation rate, leukocytosis, increased C-reactive protein, and fibrinogen [10, 11] do not exceed reference values). Treatment consists of opening and drainage of the abscess and systemic antibacterial therapy, as well as hormonal replacement therapy.

We publish one case of a primary pituitary abscess confirmed during endoscopic surgery, highlighting the clinical, diagnostic, and therapeutic aspects.

Girl M, 13 years old, vaccinated according to the calendar, acute respiratory infections 1–2 times a year, was not registered in the dispensary. At age 9, against a background of general health, a long fever of 37.0–39.0 degrees was noted; after 4 months, the fever stopped on its own, the cause remains unknown. There were courses of antibiotic therapy, and the situation normalized. At the beginning of March 2020, the whole family fell ill, presumably due to acute respiratory viral infections, had a fever of 37.5, the temperature normalized in 5 days; however, on the 6th day, the patient had repeated fever up to hectic 39.1, headache, took antibiotic therapy of a broad spectrum without pronounced result, on April 23, 2020, the vomiting started, the intensity of headaches increased. The patient underwent an outpatient brain MRI scan, which revealed a suspected pituitary cyst (craniopharyngioma?), on May 26, 2020. The patient came to the Children`s City Clinical Hospital of Moscow on her own, complaining of episodes of elevated body temperature up to hectic levels, repeated vomiting once in 3–4 days, intense headache, not relieved by analgesics, and weakness.

Для Цитирования:
76716. Bulletin of Neurology, Psychiatry and Neurosurgery. 2022;.
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