Neoplasia Video/mindmap: Six characteristics of cancer cells:
https://pathweb.nus.edu.sg/pathology-demystified/neoplasia/i-what- 1. Self-sufficient in growth factors Clinical workflow for cancer diagnosis: is-neoplasia/ 2. Insensitive to inhibitory signals 1. Biopsy performed tissue sent to patho lab pathologist 3. Resistant to apoptosis ascertains if malignant clinician decides on treatment 4. Immortal 2. After surgical excision (if done) pathologist examines the removed 5. Angiogenesis tumour to decide on grade and local stage multidisciplinary team 6. Able to invade and metastasize decides on further treatment (e.g. chemotherapy) Requires multi-step genetic alterations to overcome multiple protective mechanisms: Definition (1) Cell cycle regulatory checkpoints Neoplasm: An abnormal mass of tissue, the growth of which exceeds, (2) Tumour suppressing mechanisms and is uncoordinated with that of the normal tissues and persists in the (3) Apoptosis (cell death) & same excessive manner after cessation of the stimuli which evoked the (4) DNA repair mechanisms change. Pathogenesis Video/Mindmap: https://pathweb.nus.edu.sg/pathology- demystified/neoplasia/ii-how/ Characteristics of Benign VS Malignant tumours Benign Malignant Examples of genes involved: Appearance and behaviour Gross and microscopic features Gross and microscopic features “innocent” abnormal Remains localized – does NOT Locally invasive invade. Appearance – Microscopic (often related to tumour grade) No metastasis Metastasis (e.g. via vessels) (More: Papa Robbins 9th edition page 268-272) Treatment Amenable to local surgical Requires surgical removal excision/radio/chemo Prognosis/Outcome Patient generally survives. Death and morbidity, cachexia. However can cause significant (often) morbidity through local effects e.g. brain tumour compression
Nomenclature on tumours – how to name tumours
Mechanisms of genetic aberrations – Prognosis (Malignant tumours) Kindly refer to notes/robbins textbook for more details. Video/Mindmap: https://pathweb.nus.edu.sg/pathology- Inherited genetic aberration demystified/neoplasia/iii-clinical-effects-of-neoplasms/ - Inherited cancer syndromes, familial cancers “Acquired” genetic aberration Stage and Grade are parameters used to assess clinical aggressiveness. - Aging – Accumulation of gene mutations over the years - Physical injury – Radiation / radiotherapy Stage - size and/or extent of the tumour growth - Chemical carcinogens – Tobacco, Asbestos etc Tumour stage essentially refers to the size and/or extent of the tumour - Biological – Chronic inflammation (Chronic liver cirrhosis: growth. Clinical findings, radiological imaging (CT scans, MRI, PET scans Hepatocellular carcinoma) etc), intra-operative surgical findings and pathology reports of excised - Viral integration into host genome can cause: oncogene expression, tumours are used to stage tumours. The AJCC TNM (American Joint tumour suppressor gene inhibition, drive polyclonal proliferation of Committee on Cancer) staging system is widely used. Different lymphocytes leading to increased risk of acquiring genetic mutations tumours have different TNM staging systems according to site and /or which contribute to neoplastic transformation. tissue of origin. Ebstein-Barr Virus – Hodgkin lymphoma, Burkitt lymphoma, Nasopharyngeal CA; Grade - reflects the degree of differentiation of the tumour Human Papilloma Virus – Squamous cell carcinoma of the uterine How well the tumour cells resemble the tissue of origin. The closer the cervix resemblance, the lower the grade. In high grade tumours, the tumour - Bacterial (Helicobactor pylori: Gastric lymphoma) cells appear very abnormal and are hard recognise as a certain cell type. Effects of Neoplasia Tumour grade is thus always assessed MICROSCOPICALLY (by the Clinical Effects Video/Mindmap: pathologist) https://pathweb.nus.edu.sg/pathology-demystified/neoplasia/iii- clinical-effects-of-neoplasms/ Important Resources – do not forget: Quizzes and Media Gallery: https://pathweb.nus.edu.sg/pathology- demystified/neoplasia/1249-2/
- Know how to describe POTS/tumours grossly, distinguish grossly
between benign and malignant, and appreciate the histological characteristics of benign and malignant tumours.