Infectious Diseasess Flashcards
Describe the organ involvement in tertiary syphilis.
Describe the histological structure
of syphilitic granuloma
Occurs AFTER Latent Period of SECONDARY Lesions, about 2-3 Years AFTER 1st Exposure!
LESIONS of TERTIARY Syphilis are LESS INFECTIVE and have 2 Types:
1) SYPHILITIC GUMMMA
- Solitary, Localised, RUBBERY-Lesion
- CLAY-Line NECROSIS
- Seen in Liver, Testes, Bone + Brain
- CENTRAL Coagulative Necrosis
- ## PALISADING MFs w/ Plasma Cells, Lymph, Giant Cells + Fibroblasts2) DIFFUSE LESIONS
- WIDESPREAD Dissemination of SPIROCHETES
a) CVS Syphilis = In the THORACIC AORTA, leading to AORTIC Aneurysm
b) Neurosyphilis
- Manifests as MENINGOVASCULAR Syphilis, TABES DORSALIS or PARSES - affecting the BRAIN
Primary complexes in tuberculosis
Aka GHONS COMPLEX which is a TRIAD of:
1) PULMONARY LESION = 1-2cm SOLITARY + Found in SUBPLEURAL FOCUS in UPPER PARTS of the LUNG
2) TB Lymphangitis
PROGNOSIS:
1) Healing VIA FIBROSIS of GHONS COMPLEX
2) PROGRESSIVE Primary TB, which CONTINUES to grow / spread
3) HEMATOGENOUS TB, where BACILI ENTERS Circulation
4) PROGRESSIVE Secondary TB, where HEALED LESION is RE-ACTIVATED
List the forms of secondary tuberculosis
1) FIBROCASEOUS Tuberculosis:
- ORIGINAL AREA of TB, which HEALS at the PERIPHERY WITH a MASSIVE CENTRAL CASEOUS Necrosis Cavity
a) CAVITARY / OPEN = It can BREAK thru BRONCHUS + FORM a CAVITY - Showing a THICK FIBROUS Wall, with YELLOW NECROTIC Material and WIDESPREAD TUBERCLES
b) CHRONIC = Remains a SOFT CASEOUS Lesion , WITHOUT DRAINAGE into –> Bronchus
2) TB CASEOUS PNEUMONIA:
- TB that spreads to REST OF LUNG, where there’s an EXUDATIVE REACTION - Fibri, Polymporphs, Monocyhtes + Tubercle Bacilli
3) MILITARY TB
- TB Infection that LYMPHOHEMATOGENOUSLY SPREADS, either PULMONARY / EXTRAPULMONARY,
- Forming MILLET-SIZED Tubercles
4) TB PLEURITIS & EMPYEMA
- COMPLICATION of Secondary TB
- SEROUS / FIBRIN Exudate is HEALED VIA FIBROSIS
- There’s OBLITERATED Pleural Cavity WITH CASEOUS Material
- Develop EMPYEMA
Forms of urological tuberculosis
How do we form the names of benign and malignant mesenchymal tumours? Give at
at least three examples.
1) EPITHELIAL
0 Benign
- Squamous Papilloma
- Adenoma
0 Malignant:
- Squamous Cell Carcinoma
- Adenocarcinoma
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2) MESENCHYMAL
0 Benign
- Lipoma (Fat)
- Chondroma (Cartilage)
- Haemangioma (Blood Vessles)
- Leiomyoma (Muscle)
0 Malignant:
- Liposarcoma (Fat)
- Chondrosarcoma (Cartilage)
- Angiosarcoma (Blood Vessels)
- Leiomyosarcoma (Muscle)
- Leukaemia / Lymphoma (Haematolymphoid)
Squamous intraepithelial lesions and dysplasia. Definitions
1) SQUAMOUS INTRAEPITHELIAL LESION = This Term is USED to INDICATE the Cells from Pap Smear may be PRE-CANCEROUS
CIN 1 = Nuclear Enlargement + Hyperchromasia in BASAL 1/3 of Cells
CIN 2 = 2/3 of EPITHELIUM show NUCLEAR Changes
2) DYSPLASIA
- ABNORMAL Organisation of Cells
- Characterised by PLEOMORPHISM, Disorderly Arrangement within Epithelium + Nuclear Changes
- Consists of Enlargement, IRREGULAR Borders, HYPERChromasia of INDIVIDUAL Nuclei + INCREASED N.O of Mitotic Figures
What do the terms Main disease and Immediate cause of death mean?
MAIN DISEASE
- Disease that DIRECTLY / Via COMPLICATIONS have a GREAT Impact on Px Life
INTERMEDIATE Cause of Death
- SPECIFIC Nosological Unit (Disease Injury, Complication of Disease)
- LEADING to Cardiac / Respiratory Failure + DEATH of Px
Svetko carcinoma - macro and microscopic