Upper respiratory tract pathology Flashcards
What is the majority of histology of the URT?
Pseudostratified ciliated columnar with interspersed goblet cells
What is Kartagener’s syndrome?
Primary ciliary dymotility alongisde complete situs invertus
What is the inheritance pattern of Kartagener’s syndrome?
Autosomal recessive
What are the symptoms of primary ciliary dysmotility?
Reduced or absent mucus clearance from the lungs and subsequent susceptibility to recurrent respiratory infections. Many males will develop diminished or absent fertility and many individuals will do on to develop hearing loss and symptoms of otitis media
What are the histopathological findings in chronic rhinitis?
Atrophy of mucous glands and surface epithelium, squamous metaplasia, fibrosis
What are the histopathological findings of sinusitis?
Nasal and naso-sinal polyps
What is the most common causative agent of pharyngitis?
Streptococcus pyogenes
What are some of the severe effects of pharyngitis?
Tonsillitis, retropharyngeal abscess, peritonsillar abscess, cervical adenitis, parapharyngeal abscess, Ludwig’s angina
What is Ludwig’s angina?
Ludwig’s angina is a rare skin infection that occurs on the floor of the mouth, underneath the tongue. This bacterial infection often occurs after a tooth abscess, which is a collection of pus in the center of a tooth. It can also follow other mouth infections or injuries.
What is the cardinal triad of granulomatosis with polyangiitis?
1) Giant cell transformation
2) Arteritis/phlebitis
3) Zonal necrosis with karyorrhesis/leukocytoclasis
What is granulomatosis with polyangiitis?
Granulomatosis with polyangiitis (GPA, previously known as Wegener’s granulomatosis) is a systemic vasculitis that affects both small and medium-sized vessels. Patients typically initially suffer from a limited form that may consist of constitutional symptoms and localized manifestations such as chronic sinusitis, rhinitis, otitis media, ocular conditions, and/or skin lesions. In later stages, more serious manifestations may arise, including pulmonary complications and glomerulonephritis, although the skin, eyes, and heart may also be involved.
How is a diagnosis of GPA made?
Diagnosis is based on laboratory testing (positive for PR3-ANCA/c-ANCA), imaging, and biopsy of affected organs, which demonstrate necrotizing granulomatous inflammation.
How is GPA managed?
GPA is treated with immunosuppressive drugs, typically consisting of glucocorticoids combined with methotrexate, cyclophosphamide, or rituximab. Relapses are common.
Are the kidneys often affected?
Yes, 75% of GPA sufferers will experience kidney issues
What is the peak age of incidence?
Middle age