scholarly journals POS-153 CRESCENTIC POSTINFECTIOUS GLOMERULONEPHRITIS IN AN ADULT PATIENT WITH JUVENILE NASOPHARYNGEAL ANGIOFIBROMA: A CASE REPORT

2021 ◽  
Vol 6 (4) ◽  
pp. S61-S62
Author(s):  
S.A. MANALILI ◽  
P.N. So ◽  
A.L. Naidas ◽  
A.R. Villanueva
2021 ◽  
Vol 6 (1) ◽  
pp. 45-52
Author(s):  
Marlinda Adham ◽  
Kartika Hajarani ◽  
Lisnawati Rachmadi ◽  
Indrati Suroyo

2015 ◽  
Vol 129 (10) ◽  
pp. 1032-1035 ◽  
Author(s):  
M-L Mørkenborg ◽  
M Frendø ◽  
T Stavngaard ◽  
C Von Buchwald

AbstractBackground:Juvenile nasopharyngeal angiofibroma is a benign, vascular tumour that primarily occurs in adolescent males. Despite its benign nature, aggressive growth patterns can cause potential life-threatening complications. Juvenile nasopharyngeal angiofibroma is normally unilateral, originating from the sphenopalatine artery, but bilateral symptoms can occur if a large tumour extends to the contralateral side of the nasopharynx. This paper presents the first reported case of true bilateral extensive juvenile nasopharyngeal angiofibroma involving clinically challenging pre-surgical planning and surgical strategy.Case report:A 21-year-old male presented with increasing bilateral nasal obstruction and discharge. Examination revealed tumours bilaterally and imaging demonstrated non-contiguous tumours. Pre-operative angiography showed strictly ipsilateral vascular supplies requiring bilateral embolisation. Radical removal performed as one-step, computer-assisted functional endoscopic sinus surgery was performed. The follow-up period was uncomplicated.Conclusion:This case illustrates the importance of suspecting bilateral juvenile nasopharyngeal angiofibroma in patients presenting with bilateral symptoms. Our management, including successful pre-operative planning, enabled one-step total removal of both tumours and rapid patient recovery.


1979 ◽  
Vol 87 (1) ◽  
pp. 42-46 ◽  
Author(s):  
Paul J. Donald

Malignant degeneration in a juvenile nasopharyngeal angiofibroma has been reported in the literature in only four patients. All of these persons had been previously treated for cure with gamma irradiation. The case report of a 47-year-old man with a 31-year history of nasal obstruction is presented. A recurrence excised 18 months after initial removal of an angiofibroma revealed the surprising diagnosis of fibrosarcoma.


BioMedicine ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 41-44
Author(s):  
Mojtaba Mohammadi Ardehali ◽  
Shirin Irani ◽  
Mohammadreza Firouzifar

2021 ◽  
Vol 14 (4) ◽  
pp. e242785
Author(s):  
Sheryll Anne Manalili ◽  
Paolo Nikolai So ◽  
Maria Ana Louise Naidas ◽  
Anthony Russell Villanueva

Crescentic glomerulonephritis is usually associated with an acute nephritic syndrome with rapidly declining renal function. Postinfectious cases usually have a higher possibility of recovery. Juvenile nasopharyngeal angiofibroma (JNA) is a rare, locally aggressive tumour affecting mostly young men. A 28-year-old man presented with recurrent JNA initially excised 2 years prior. The patient was initially managed as a case of airway obstruction and pneumonia. He developed tea-coloured urine, oedema and acute kidney failure requiring dialysis while awaiting surgery. Urine and immunological studies (low C3, negative antineutrophil cytoplasmic antibody and antinucleosomal antibody and high antistreptolysin O) suggested a nephritic aetiology. Nasopharyngeal swab cultures of the mass revealed gram-negative organisms. Kidney biopsy showed diffuse proliferative glomerulonephritis compatible with a postinfectious glomerulonephritis with 77% cellular crescents. The mass was excised with histopathology consistent with JNA. The patient was eventually discharged off dialysis.


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