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SEMINAR TOPIC –
GRANULOMATOUS
DISEASES OF NOSE
NAME - MAYANK SAH
MBBS BATCH 2020
TYPES -
BACTERIAL INFECTIONS
FUNGAL INFECTIONS
PARASITIC INFECTIONS
INFLAMMATORY / AUTOIMMUNE
NOTE - GRANULOMATOUS LESIONS OF NOSE ARE NOT SPECIFIC FEATURE OF
ALL MENTION DISEASE THEY CAN BE SECONDARY TO SYSTEMIC DISEASES
 BACTERIAL INFECTIONS
1) RHINOSCLEROMA –
It is a chronic granulomatous disease caused by Klebsiella
rhinoscleromatis /Frisch Bacillus
More common in north than in south
PATHOLOGY
• Starts from nose and extends to nasopharynx ,oropharynx, larynx
[subglottic region] trachea ,bronchi
• Ratio is 1:1 for male and female
 Clinical features-
Atrophic stage –
• Foul smell
• Nasal discharge
• Crusting
Granulomatous stage –
• Painless nodules
• Woody feel/hebra/Hard [due to granuloma] of external nose and
upper lip
Cicatricial stage
• Stenosis of nares [Tapir nose ]
• Subglottic stenosis and fibrosis[difficulty breathing]
 Diagnosis-
• Biopsy-shows MIKULICZ CELLS AND RUSSEL BODIES
• Mikulicz cells are macrophages that phagocytosed the bacteria forming large
foamy cells
• Russel bodies are plasma cells with eosinophilic inclusion bodies
• Culture of the organism isolated from biopsy
TREATMENT-
• Streptomycin 1g/day and Tetracycline 2g/day at least for 6 weeks
• Ciprofloxacin, rifampin, steroids [to avoid fibrosis]
Note –treatment is stopped only when two consecutive culture are negative
• Surgical establish airway and correct deformity –tracheostomy
2)TUBERCULOSIS -
• It is rarely presented as primary tuberculosis of nose but more often
as secondary to lung tuberculosis
• Site involved-anterior nasal septum and anterior part of inferior
turbinate
• Nodal infiltration
• Ulceration
• Perforation of the nasal septum (cartilaginous part)
 Diagnosis-
• Biopsy
• Z-N Staining for Acid Fast Bacilli
 Treatment-
• Anti tubercular drugs like
• Isoniazid ,rifampicin ,ethambutol ,pyrazinamide
 Cutaneous lesions of Tuberculosis
 LUPUS VALGARIS –commonly seen in immunocompromised patients
 Like organ transplant ,HIV etc
 Characteristic features – apple jelly nodules [brown colour , no blanch on pressure]
 Presents as chronic vestibulitis
 Perforation of cartilaginous septum can be seen
 Treatment same as for tuberculosis
3)SYPHILIS-( cause treponema pallidum)
Types –
a) Acquired –
• Primary –rare and presents with painless ulcer of vestibule
• Secondary-rarely recognize because presents as simple rhinitis ,snail
track ulcer can be seen
• Tertiary-Gummous lesions seen
• Features –septum destroy[bony part]
• Saddling of nose
• Crusting and offensive nasal discharge
B)congenital
• Two forms-
• a) early- in the first three months of life manifests as
‘snuffles’(catarrhal rhinitis )
• b)late –around puberty similar as tertiary stage of acquired gummous
lesions
Diagnosis –
• Serology test [ VDRL]
• Biopsy stain for treponema pallidum
Treatment
• Penicillin I.M every week for 3 weeks
• Nasal irrigation by alkaline solution
4)LEPROSY-(Not isolated to nose but systemic disease)
• Common in tropical areas
• Loss of sensations , neuropathies
• Cause –Mycobacterium leprae
• Sites – from anterior part of septum
• Feature –initial
• Nasal discharge
• Red swollen mucosa
-Late
Perforation and ulceration
Destruction of nasal spine
 Diagnosis
• Biopsy –scrapings of nasal mucosa
• Histological finding lepra cells acid fast bacilli can be seen
Treatment –
• Dapsone ,rifampin, isoniazid
• Reconstruction is done once disease is subsided
 PARASITIC INFECTIONS -
RHINOSPORIDIOSIS-
• Chronic infection caused byRHINOSPORIDIUM SEEBERI
• It is an aquatic protistan parasite earlier it was considered as fungus
• More common in southern part of India
• Acquired through contaminated water and ponds frequented by
animals
CLINICAL FEATURES-
• Not confined to any part can be seen any ware
• Leafy , polypoidal ,pink ,Strawberry with white dots/mulberry type
presentation
• Recurrent Epistaxis is associated with the disease
• Skin nodules and hypertrophy of turbinate is seen
 Diagnosis-
• Biopsy is not preferred as it is a very vascular structure instead
• Smear is prepared to visualize the round shaped sporangia
under microscope
Treatment –
• Surgical excision of complete mass and cauterization on base is
done ,may reoccur (wide excision )
• Medication –dapsone but not very effective
 FUNGAL INFECTIONS -
ASPERGILLOSIS-
• Caused by Aspergillus niger in immunocompromised patient
• Systemic or intracranial involvement can be fatal either due to
infection or due to side effects of the drugs
Clinical features –
• Black/ grey membrane seen over nasal mucosa
• Sinus examination shows semisolid cheesy-white material
Treatment –
• Antifungal drugs like Amphotericin B
 MUCORMYCOSIS-
• Involve cribriform plate , brain ,meninges, nose and sinuses
• Rapid destruction of structure thrombosis and invades artery
due to which the fatality rate is high if not treated
• Was commonly seen during COVID-19 in immunosuppressive
patient and long term use of steroids
• “Black fungus” name was given due to black necrotic material
seen areas (rhino-orbito-cerebral)
Treatment –
• Amphotericin B
• Surgical debriment
 INFLAMMATORY/AUTOIMMUNE -
WEGENER’S GRANULOMATOSIS/GRANULOMATOSIS WITH
POLYANGITIS
• Systemic disease involve mainly upper airways ,lungs ,kidney and skin
Clinical features-
• 80% of the patient will present with problem –
• Nasal obstruction due to crusting
• Perforation of septum (bony+cartilage)
• Saddling of nose and blood tinged discharge ,hemoptysis
• Renal failure is the main cause of death in patients
• Gingival hyperplasia –strawberry like –pathognomonic rare
 Diagnosis-
• Done by c-ANCA
• X-Ray may show single or multiple cavity lesions
• CT scan will show pulmonary infiltration and nodules
• Biopsy is diagnostic showing necrotizing granulomatous vasculitis
Treatment –
• Immunosuppressive drugs –cyclophosphamide
• Steroids both are found effective
 SARCOIDOSIS-( Rare nasal involvement 1-4%)
• Resembles TB on histology but with absence of caseation
• Involves lungs, lymph nodes and skin
• Heerfordt syndrome –It is a rare subacute version
• B/L parotid enlargement ,facial palsy , anterior uveitis
• Patient presents with nasal obstruction ,pain, sometime epistaxis ,saddling
of nose (bony) ,perforation septum
• Strawberry appearance of nasal mucosa
• Lupus pernio-violaceous affection of skin of nose and cheek
Treatment-
• Systemic steroids
• Nasal sprays, Hydroxychloroquine
 T/NK –cell Lymphoma-
• Neoplastic lesion with granulomas
• Features-midline malignant lesion , lethal granuloma
• Unlike Wegener’s it do not involve lung and kidneys
• Diagnostic –biopsy and CD-56 marker
• Treatment –
• Chemotherapy
• Radiation therapy
• Calcium supplement as calcium is washed out in this disease
TOPIC – GRANULOMATOUS  DISEASES  OF  NOSE

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TOPIC – GRANULOMATOUS DISEASES OF NOSE

  • 1. SEMINAR TOPIC – GRANULOMATOUS DISEASES OF NOSE NAME - MAYANK SAH MBBS BATCH 2020
  • 2. TYPES - BACTERIAL INFECTIONS FUNGAL INFECTIONS PARASITIC INFECTIONS INFLAMMATORY / AUTOIMMUNE NOTE - GRANULOMATOUS LESIONS OF NOSE ARE NOT SPECIFIC FEATURE OF ALL MENTION DISEASE THEY CAN BE SECONDARY TO SYSTEMIC DISEASES
  • 3.  BACTERIAL INFECTIONS 1) RHINOSCLEROMA – It is a chronic granulomatous disease caused by Klebsiella rhinoscleromatis /Frisch Bacillus More common in north than in south PATHOLOGY • Starts from nose and extends to nasopharynx ,oropharynx, larynx [subglottic region] trachea ,bronchi • Ratio is 1:1 for male and female
  • 4.  Clinical features- Atrophic stage – • Foul smell • Nasal discharge • Crusting Granulomatous stage – • Painless nodules • Woody feel/hebra/Hard [due to granuloma] of external nose and upper lip Cicatricial stage • Stenosis of nares [Tapir nose ] • Subglottic stenosis and fibrosis[difficulty breathing]
  • 5.  Diagnosis- • Biopsy-shows MIKULICZ CELLS AND RUSSEL BODIES • Mikulicz cells are macrophages that phagocytosed the bacteria forming large foamy cells • Russel bodies are plasma cells with eosinophilic inclusion bodies • Culture of the organism isolated from biopsy TREATMENT- • Streptomycin 1g/day and Tetracycline 2g/day at least for 6 weeks • Ciprofloxacin, rifampin, steroids [to avoid fibrosis] Note –treatment is stopped only when two consecutive culture are negative • Surgical establish airway and correct deformity –tracheostomy
  • 6. 2)TUBERCULOSIS - • It is rarely presented as primary tuberculosis of nose but more often as secondary to lung tuberculosis • Site involved-anterior nasal septum and anterior part of inferior turbinate • Nodal infiltration • Ulceration • Perforation of the nasal septum (cartilaginous part)
  • 7.  Diagnosis- • Biopsy • Z-N Staining for Acid Fast Bacilli  Treatment- • Anti tubercular drugs like • Isoniazid ,rifampicin ,ethambutol ,pyrazinamide  Cutaneous lesions of Tuberculosis  LUPUS VALGARIS –commonly seen in immunocompromised patients  Like organ transplant ,HIV etc  Characteristic features – apple jelly nodules [brown colour , no blanch on pressure]  Presents as chronic vestibulitis  Perforation of cartilaginous septum can be seen  Treatment same as for tuberculosis
  • 8. 3)SYPHILIS-( cause treponema pallidum) Types – a) Acquired – • Primary –rare and presents with painless ulcer of vestibule • Secondary-rarely recognize because presents as simple rhinitis ,snail track ulcer can be seen • Tertiary-Gummous lesions seen • Features –septum destroy[bony part] • Saddling of nose • Crusting and offensive nasal discharge
  • 9. B)congenital • Two forms- • a) early- in the first three months of life manifests as ‘snuffles’(catarrhal rhinitis ) • b)late –around puberty similar as tertiary stage of acquired gummous lesions Diagnosis – • Serology test [ VDRL] • Biopsy stain for treponema pallidum Treatment • Penicillin I.M every week for 3 weeks • Nasal irrigation by alkaline solution
  • 10. 4)LEPROSY-(Not isolated to nose but systemic disease) • Common in tropical areas • Loss of sensations , neuropathies • Cause –Mycobacterium leprae • Sites – from anterior part of septum • Feature –initial • Nasal discharge • Red swollen mucosa -Late Perforation and ulceration Destruction of nasal spine
  • 11.  Diagnosis • Biopsy –scrapings of nasal mucosa • Histological finding lepra cells acid fast bacilli can be seen Treatment – • Dapsone ,rifampin, isoniazid • Reconstruction is done once disease is subsided
  • 12.  PARASITIC INFECTIONS - RHINOSPORIDIOSIS- • Chronic infection caused byRHINOSPORIDIUM SEEBERI • It is an aquatic protistan parasite earlier it was considered as fungus • More common in southern part of India • Acquired through contaminated water and ponds frequented by animals CLINICAL FEATURES- • Not confined to any part can be seen any ware • Leafy , polypoidal ,pink ,Strawberry with white dots/mulberry type presentation • Recurrent Epistaxis is associated with the disease • Skin nodules and hypertrophy of turbinate is seen
  • 13.  Diagnosis- • Biopsy is not preferred as it is a very vascular structure instead • Smear is prepared to visualize the round shaped sporangia under microscope Treatment – • Surgical excision of complete mass and cauterization on base is done ,may reoccur (wide excision ) • Medication –dapsone but not very effective
  • 14.  FUNGAL INFECTIONS - ASPERGILLOSIS- • Caused by Aspergillus niger in immunocompromised patient • Systemic or intracranial involvement can be fatal either due to infection or due to side effects of the drugs Clinical features – • Black/ grey membrane seen over nasal mucosa • Sinus examination shows semisolid cheesy-white material Treatment – • Antifungal drugs like Amphotericin B
  • 15.  MUCORMYCOSIS- • Involve cribriform plate , brain ,meninges, nose and sinuses • Rapid destruction of structure thrombosis and invades artery due to which the fatality rate is high if not treated • Was commonly seen during COVID-19 in immunosuppressive patient and long term use of steroids • “Black fungus” name was given due to black necrotic material seen areas (rhino-orbito-cerebral) Treatment – • Amphotericin B • Surgical debriment
  • 16.  INFLAMMATORY/AUTOIMMUNE - WEGENER’S GRANULOMATOSIS/GRANULOMATOSIS WITH POLYANGITIS • Systemic disease involve mainly upper airways ,lungs ,kidney and skin Clinical features- • 80% of the patient will present with problem – • Nasal obstruction due to crusting • Perforation of septum (bony+cartilage) • Saddling of nose and blood tinged discharge ,hemoptysis • Renal failure is the main cause of death in patients • Gingival hyperplasia –strawberry like –pathognomonic rare
  • 17.  Diagnosis- • Done by c-ANCA • X-Ray may show single or multiple cavity lesions • CT scan will show pulmonary infiltration and nodules • Biopsy is diagnostic showing necrotizing granulomatous vasculitis Treatment – • Immunosuppressive drugs –cyclophosphamide • Steroids both are found effective
  • 18.  SARCOIDOSIS-( Rare nasal involvement 1-4%) • Resembles TB on histology but with absence of caseation • Involves lungs, lymph nodes and skin • Heerfordt syndrome –It is a rare subacute version • B/L parotid enlargement ,facial palsy , anterior uveitis • Patient presents with nasal obstruction ,pain, sometime epistaxis ,saddling of nose (bony) ,perforation septum • Strawberry appearance of nasal mucosa • Lupus pernio-violaceous affection of skin of nose and cheek Treatment- • Systemic steroids • Nasal sprays, Hydroxychloroquine
  • 19.  T/NK –cell Lymphoma- • Neoplastic lesion with granulomas • Features-midline malignant lesion , lethal granuloma • Unlike Wegener’s it do not involve lung and kidneys • Diagnostic –biopsy and CD-56 marker • Treatment – • Chemotherapy • Radiation therapy • Calcium supplement as calcium is washed out in this disease