Seemingly neoplastic destructive lesion of maxillary sinus, eroding the bone and extending into skull base- Atypical Rhinoscleromaor Antroscleroma

  • Dr. Sunitha Shankaralingappa Columbia Asia Hospital, Hebbal, Bangalore, Karnataka, India
  • Dr. Santhosh Shivaswamy Columbia Asia Hospital, Hebbal, Bangalore, Karnataka, India
Keywords: Rhinoscleroma, Klebsiella rhinoscleromatis, sinus involvement, early recurrence, antibiotic resistance

Abstract

Rhinoscleroma (RS) is a chronic granulomatous infectious disease predominantly affecting the nose and upper respiratory tract caused by Klebsiella rhinoscleromatis (KR), a gram negative diplobacillus. In India, it is prevalent in Northern and central parts. Belinov, in 1932 proposed the term “scleromarespiratorium” as the disease process may involve not only the upper, but also lower respiratory pathways. A 35 year old male from South India, presented with mass in the right maxillary and ethmoid sinuses eroding the bone, extending into infratemporal fossa and skull base, clinically mimicking malignancy. Histopathological examination confirmed rhinoscleroma. Nasal cavity free, isolated ipsilateral involvement of sinusesmakes this case interesting and one among the few case reports reported in the past. Rhinoscleroma should be differentiated from other granulomatous conditions and neoplastic diseases like lymphoma & Sinonasal carcinoma. Correct diagnosis is very crucial as sinus-positive cases are linked with antibiotic resistance and early recurrence after medical treatment.

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Seemingly neoplastic destructive lesion of maxillary sinus, eroding the bone and extending into skull base- Atypical Rhinoscleromaor Antroscleroma
CITATION
DOI: 10.17511/jopm.2018.i02.11
Published: 2018-06-30
How to Cite
Dr. Sunitha Shankaralingappa, & Dr. Santhosh Shivaswamy. (2018). Seemingly neoplastic destructive lesion of maxillary sinus, eroding the bone and extending into skull base- Atypical Rhinoscleromaor Antroscleroma. Tropical Journal of Pathology and Microbiology, 4(2), 176-180. https://doi.org/10.17511/jopm.2018.i02.11
Section
Case Report