Fever as the First Clue: an Atypical Case of Occult Brown Tumor

Main Article Content

Ashok Arbat
https://orcid.org/0000-0002-8694-2597
Diti Gandhasiri
https://orcid.org/0000-0001-8257-3205
Sweta Chourasia
https://orcid.org/0000-0001-7204-8546
Swapnil Bakamwar
https://orcid.org/0000-0002-1143-0319
Parimal Deshpande
https://orcid.org/0000-0002-3391-703X

Abstract

A 46-year-old asian male presented with throat pain, hoarseness, dry cough and persistent high-grade fever unresponsive to antibiotics. Imaging showed left upper lobe consolidation and bronchoscopy revealed no infectious cause. Although the patient initially improved with intravenous antibiotics, fever recurred post-discharge, prompting further evaluation. Imaging identified multiple lytic bone lesions, initially suggestive of malignancy. However, bone biopsy revealed osteitis fibrosa cystica (Brown tumor), indicating metabolic bone disease. Laboratory tests showed markedly elevated parathyroid hormone (PTH) levels with high-normal serum calcium, confirming primary hyperparathyroidism. PET-CT and parathyroid scintigraphy localized a left inferior parathyroid adenoma. Surgical resection of the adenoma led to normalization of PTH levels and resolution of systemic symptoms, including fever. This case highlights fever as an atypical presentation of primary hyperparathyroidism and underscores the importance of considering endocrine disorders in cases of pyrexia of unknown origin, especially when conventional infectious and malignant causes are excluded.

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Fever as the First Clue: an Atypical Case of Occult Brown Tumor. (2025). Respirar, 17(3), 356–365. https://doi.org/10.55720/respirar.17.3.14

References

Diacinti D, Cipriani C, Biamonte F et al. Imaging technologies in the differential diagnosis and follow-up of brown tumor in primary hyperparathyroidism: Case report and review of the literature. Bone Rep 2020;14:100745. Doi: 10.1016/j.bonr.2020.100745.

Guedes A, Becker RG, Nakagawa SA, Guedes AAL. Update on brown tumor of hyperparathyroidism. Rev Assoc Med Bras (1992) 2024;70(suppl 1): e2024S132. Doi: 10.1590/1806-9282.2024S132.

Zhong Y, Huang Y, Luo J, Ye Y. Misdiagnosis of brown tumour caused by primary hyperparathyroidism: a case report with literature review. BMC Endocr Disord 2022;22(1):66. Doi: 10.1186/s12902-022-00971-2.

Rosenberg AE, Nielsen GP. Giant cell containing lesions of bone and their differential diagnosis. Curr Diagn Pathol 2001;7:235-246. Doi: 10.1054/cdip.2001.0080.

Etemadi J, Mortazavi-Khosrowshahi M, Ardalan MR, Esmaili H, Javadrashid R, Shoja MM. Brown tumor of hyperparathyroidism masquerading as central giant cell granuloma in a renal transplant recipient: a case report. Transplant Proc 2009;41(7):2920-2. Doi: 10.1016/j.transproceed.2009.07.040.

Khomariyah E, Purnamasari Y, Basuki MH, Massora S. Diagnostic challenge of the brown tumors in developing country: A case series. Int J Surg Case Rep 2024;123:110221. Doi: 10.1016/j.ijscr.2024.110221.

Samir K. El-Mofty, Chapter 9 - Bone Lesions. En: Douglas R. Gnepp. Diagnostic Surgical Pathology of the Head and Neck (Second Edition), W.B. Saunders, 2009; pp. 729-784.

Tayfun H, Metin O, Hakan S, Zafer B, Vardar AF. Brown tumor as an unusual but preventable cause of spinal cord compression: Case report and review of the literature. Asian J Neurosurg 2014;9(1):40-44. Doi: 10.4103/1793-5482.131074.

Anastasopoulou C, Naji Rad S, Barnett MJ et al. Osteitis Fibrosa Cystica. StatPearls. Treasure Island (FL), 2025. [Internet]. [Consultado 6 feb 2025]. Disponible en: https://www.ncbi.nlm.nih.gov/books/NBK559097/.

Choi JH, Kim KJ, Lee YJ et al. Primary Hyperparathyroidism with Extensive Brown Tumors and Multiple Fractures in a 20-Year-Old Woman. Endocrinol Metab (Seoul) 2015;30(4):614-619. Doi: 10.3803/EnM.2015.30.4.614.

Can Ö, Boynueğri B, Gökçe AM, Özdemir E, Ferhatoğlu F, Canbakan M. Brown Tumors: A Case Report and Review of the Literature. Case Rep Nephrol Dial 2016;6(1):46-52. Doi:10.1159/000444703.

Wasiak M, Popow M, Bogdańska M, Starzyńska-Kubicka A, Małdyk P, Wasilewski P. Treatment of pathological fractures due to brown tumours in a patient with hyperparathyroidism and lack of parafibromin expression - A case report. Trauma Case Rep 2020;30:100367. Doi: 10.1016/j.tcr.2020.100367.

Pinto M, Gaffrée, Santos R et al. Brown tumour revealed: A literature review with a case study. Biomed J Sci & Tech 2017;1:7. Doi : 10.26717/BJSTR.2017.01.000587.

Arsalanizadeh B, Westacott R. Osteoclastomas ('brown tumours') and spinal cord compression: a review. Clin Kidney J 2013;6(2):220-3. Doi: 10.1093/ckj/sft021.

Antin F, Bakhos D, Jegoux F, Merkouza M, Laccourreye L. Maxillofacial brown tumours: Series of 5 cases. Eur Ann Otorhinolaryngol Head Neck Dis 2018;135(4):227-230. Doi: 10.1016/j.anorl.2018.03.005.

Esselmani H, Aimrane A, Chatoui H, El Hiba O, Najimi M, Merzouki M. Severe Headache and Deterioration of Vision in Left Eye in a Chronic Hemodialysis Patient Revealing a Brown Tumor of Sphenoid Sinus. Neurol Int 2025;17(2):22. Doi: 10.3390/neurolint17020022.

Zhou Z, Shi Y, Li C, Wang W. Primary hyperparathyroidism-induced brown tumors caused by parathyroid carcinoma: a case report and literature review. J Int Med Res 2022;50(9):03000605221123668. Doi: 10.1177/03000605221123668.

Qaisi M, Loeb M, Montague L, Caloss R. Mandibular Brown Tumor of Secondary Hyperparathyroidism Requiring Extensive Resection: A Forgotten Entity in the Developed World? Case Rep Med 2015;2015:567543. Doi: 10.1155/2015/567543.

Chatterji P, Rastogi R, Mukherjee Y, Jain R. Brown Tumor of Mandible—A Rare Presenting Complaint of Hyperparathyroidism. J Maxillofac Oral Surg 2024. Doi: 10.1007/s12663-024-02413-z

Dinoi E, Prete A, Sardella C et al. The challenge of the differential diagnosis between brown tumors and metastases in parathyroid carcinoma: a case report. Front Endocrinol (Lausanne) 2024;15:1414896. Doi: 10.3389/fendo.2024.1414896.

Herrera Ortiz AF, Olarte L, Del Castillo V, Duarte JN, Rojas J, Aguirre D. Brown tumors mimicking multiple myeloma: A case report. Radiol Case Rep 2024;20(1):841-845. Doi: 10.1016/j.radcr.2024.10.055.

Diacinti D, Cipriani C, Biamonte F et al. Imaging technologies in the differential diagnosis and follow-up of brown tumor in primary hyperparathyroidism: Case report and review of the literature. Bone Rep 2020;14:100745. Doi: 10.1016/j.bonr.2020.100745.

Erdem H, Baymakova M, Alkan S et al. Classical fever of unknown origin in 21 countries with different economic development: an international ID-IRI study. Eur J Clin Microbiol Infect Dis 2023;42(4):387-398. Doi: 10.1007/s10096-023-04561-5.

Blair DC, Fekety FR. Primary hyperparathyroidism presenting as fever of unknown origin with unremitting headache. Ann Intern Med 1979;91(4):575-6. Doi: 10.7326/0003-4819-91-4-575.

Nagpure KB, Kumbhalkar S, Dube A, Indu S. Fever of Unknown Origin: A Rare Presentation of Parathyroid Carcinoma. Cureus 2024;16(12):e75868. Doi: 10.7759/cureus.75868.

Conti B, Tabarean I, Andrei C, Bartfai T. Cytokines and fever. Front Biosci 2004;9:1433-49. Doi: 10.2741/1341.

Piciucchi S, Barone D, Gavelli G, Dubini A, Oboldi D, Matteuci F. Primary hyperparathyroidism: imaging to pathology. J Clin Imaging Sci 2012;2:59. Doi: 10.4103/2156-7514.102053.

Cartwright C, Anastasopoulou C. Hungry Bone Syndrome. StatPearls. Treasure Island (FL), 2025. [Internet]. [Consultado 6 feb 2025]. Disponible en: https://www.ncbi.nlm.nih.gov/books/NBK549880/

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