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Contents

Preface  ix
Acknowledgements xi

1. INTRODUCTION TO ONCOLOGY................................................................. 1–10


Theory 2
Multiple Choice Questions  9
Answers with Explanations  9
AIIMS New Pattern 2019 Model Questions  10

2. PATHOGENESIS OF NEOPLASIA............................................................... 11–27


Theory 12
Multiple Choice Questions  24
Answers with Explanations  24
AIIMS New Pattern 2019 Model Questions  26

3. MICORBIOLOGY IN CANCERS..................................................................... 29–37


Theory 30
AIIMS New Pattern 2019 Model Questions  37

4. HEMATO-ONCOLOGY................................................................................... 39–68
Theory 40
Multiple Choice Questions  66
Answers with Explanations  68

5. HEAD AND NECK CANCERS (Including Oral Cancers, Secondaries Neck)........ 69–89
Theory 70
Multiple Choice Questions  85
Answers with Explanations  86
AIIMS New Pattern 2019 Model Questions  89

6. EAR, NOSE AND THROAT.......................................................................... 91–114


Theory 92
Multiple Choice Questions  111
Answers with Explanations  113
AIIMS New Pattern 2019 Model Questions  114
7. THYROID CANCERS................................................................................... 115–124
Theory 116
Multiple Choice Questions  123
Answers with Explanations  123
AIIMS New Pattern 2019 Model Questions  124
xiv
8. BREAST CANCERS..................................................................................... 125–148
Theory 126
Multiple Choice Questions  146
Answers with Explanations  146
AIIMS New Pattern 2019 Model Questions  148

9. GIT CANCERS.............................................................................................. 149–176


Theory 150
Multiple Choice Questions  172
Answers with Explanations  173
AIIMS New Pattern 2019 Model Questions  176

10. HEPATOBILIARY AND PANCREATIC CANCERS................................. 177–200


Theory 178
Multiple Choice Questions  196
Answers with Explanations  197
AIIMS New Pattern 2019 Model Questions  199

11. UROLOGY MALIGNANCIES..................................................................... 201–237


Theory 202
Multiple Choice Questions  235
Answers with Explanations  235
AIIMS New Pattern 2019 Model Questions  237

12. THORACIC TUMORS.................................................................................. 239–250


New SARP Series TUMOR

Theory 240
Multiple Choice Questions  247
Answers with Explanations  248
AIIMS New Pattern 2019 Model Questions  250

13. BRAIN TUMORS.......................................................................................... 251–259


Theory 252
Multiple Choice Questions  258
Answers with Explanations  258
AIIMS New Pattern 2019 Model Questions  259
14. SOFT TISSUE SARCOMA.......................................................................... 261–276
Theory 262
Multiple Choice Questions  274
Answers with Explanations  274
AIIMS New Pattern 2019 Model Questions  276
xv
15. SKIN TUMORS.............................................................................................. 277–304
Theory 278
Multiple Choice Questions  302
Answers with Explanations  302
AIIMS New Pattern 2019 Model Questions  304

16. PEDIATRIC SOLID TUMORS..................................................................... 305–200


Theory 306
AIIMS New Pattern 2019 Model Questions  316

17. ENDOCRINE TUMORS (EXCLUDING THYROID)................................. 317–326


Theory 318
Multiple Choice Questions  325
Answers with Explanations  325
AIIMS New Pattern 2019 Model Questions  326

18. GYNECOLOGICAL TUMORS..................................................................... 327–382


Theory 328
Multiple Choice Questions  375
Answers with Explanations  380
AIIMS New Pattern 2019 Model Questions  382

19. ORTHOPEDIC TUMORS............................................................................. 383–405


Theory 384
Multiple Choice Questions  403
Answers with Explanations  404
AIIMS New Pattern 2019 Model Questions  405

20. CHEMOTHERAPY DRUGS......................................................................... 407–422


Theory 408

21. RADIOTHERAPY PRINCIPLES................................................................ 423–431


Contents

Theory 424

22. AJCC 8TH EDITION: UPDATES............................................................... 433–440


Theory 434
BASICS IN ONCOLOGY
„„ MC site of primary for bone metastasis: CA Prostate*
„„ MC tumor metastasize to bone in females: CA Breast*
„„ Osteolytic bone mets: Kidney Tumors**
„„ Osteoblastic bone mets: Prostate Tumors**
MC site of primary for Brain secondary- Lungs* followed by breast
2 „„
„„ Latest MC cancer in males: Prostate > Lung > Colorectal (PLC)
„„ Latest MC cancer in females: Breast > Lung > Colorectal (BLC)
„„ Cancer deaths in males: Lung > Prostate
„„ Cancer deaths in females: Lung > Breast
„„ Osteoblastic secondaries in males is mostly due to Cancer Prostate*
„„ Osteoblastic secondaries in females is mostly due to Cancer Breast*
„„ Most effective radiosensitiser: Oxygen
„„ Amifostine: Radioprotector*
„„ Most sensitive phase of cell cycle to Radiation: G2 M > G2
„„ Most resistant phase of cell cycle to radiation: End of S phase

Distant Metastasis
 MC site of distant metastasis from lung Ca—Adrenals *next is Liver, Brain
 MC site for distant metastasis from Breast Ca—Vertebrae
 MC site for distant metastasis from Bladder Ca—Lung*
 MC site for distant metastasis from Colorectal Ca—Liver*
 MC site for distant metastasis from Melanoma (cutaneous)—Skin/subcutaneous tissue/Lung*
 MC site for distant metastasis from Melanoma (ocular)—Liver*
 MC site for distant metastasis from Prostate-Bones*
 MC site for distant metastasis from Soft tissue sarcoma—Lung*
 MC site for distant metastasis from Testis Ca—Lung*
 MC site for distant metastasis from Thyroid Ca—Bone*, Lung*
 Metastasis to lung is most commonly from—Breast Ca*

Author Punch
 CA- 19-9 : Pancreatic cancer tumor marker*
 CEA: Tumor marker for Colo rectal cancers,
 AFP: Tumor marker for HCC*
 PIVKA: Latest tumor marker for HCC*
 Calcitonin: Tumor marker for follow up of medullary cancer.
New SARP Series TUMOR

GENERAL CONCEPTS IN TUMORS AND MANAGEMENT OF TUMORS


Diagnosis of Cancer
„„ Clinical
„„ Cytology
„„ Histopathology
„„ Immunology
„„ Genetics
„„ Radiology
„„ Tumor markers
Treatment of Cancer
„„ Locoregional
zz Surgery / Radiotherapy
„„ Systemic
zz Chemotherapy
zz Hormones
zz Immunological agents 3
zz Targeted therapy

PRINCIPLES OF CANCER SURGERY


„„ Margin negativity in three dimensions
„„ Excision with regional lymph nodes in toto wherever applicable
„„ Minimise tumour spillage
„„ Excise previous scars and drain sites

RADIATION THERAPY IN CANCER


„„ Radiation therapy (RT/RTx/(XRT) is therapy using ionising radiation
„„ It is generally used as part of cancer treatment to control or kill malignant cells and is delivered by a linear accelerator.

Types of Radiotherapy (RT)


„„ Teletherapy: Beams of radiation generated at far off distance and aimed at a tumor in the patient . This is the
commonly used mode of (RT)
„„ Brachytherapy: (RT) implanted directly into tumor.
„„ Systemic (RT): Radio nuclides targeted by some method

CONCEPTS OF RADIOBIOLOGY
„„ Radiation dose: SI unit of absorbed radiation dose is Gray(Joule/Kg)
„„ Fractionation: Fractionation of treatment allows recovery of normal tissues while depleting the no. of surviving

Chapter 1  Introduction to Oncology


tumor cells.

Chemoradiation
„„ Radiation increases the cellular uptake of platinum.
„„ Hydroxyurea preferentially kills cells in the radioresistant S phase of cell cycle
„„ The G2/M phase of cell cycle is the most radiosensitive portion of cell cycle.
„„ Paclitaxel sensitizes cells in the G2/M phase
„„ Some chemotherapy drugs can recall irradiated volumes by erythema on the skin or by production of pulmonary
radiations, e.g. Adriamycin. This is referred to as radiation recall.

Radiation Types
Electromagnetic Radiations
„„ X rays
„„ Gamma rays
Multiple Choice Questions
1. Tumor lysis Syndrome is characterised by all 3. Prefix symbol used to describe the administration
except? (AIIMS Nov 2017) of neo-adjuvant treatment given in colorectal
a. Hyperuricemia cancer is? (FMGE Pattern 2017)
b. Hypercalcemia a. h
9
c. Hyperkalemia b. p
d. Hyperphosphatemia c. y
2. A child with cancer to monitor Tumor lysis d. z
syndrome which of the following investigations 4. Cancericidal solution is
need to be done? (JIPMER Nov 2017)  (Recent Pattern 2017)
a. Urea, Creatinine, Chloride and Ca2+, K+ a. 1% cetrimide
b. Urea, Creatinine, Phosphate and Ca2+, K+ b. Phenol
c. Urea, Creatinine, Magnesium and Ca2+, K c. Formaldehyde
d. Urea, Calcium, Ammonia d. 10% saline

Answers with Explanations


1. Ans. (b)  Hypercalcemia preoperative therapy, the TNM classification
[Ref: Surgery Sixer 2nd Edition Page 944] of the International Union Against Cancer and
American Joint Committee on Cancer includes a
•• Tumor lysis syndrome is characterised by Hypo-
prefix “yc,” with yc used for clinical and “yp” for
calcemia and not by Hypercalcemia**
pathologic classifications.
•• The ypTNM classification deals with the extent of
2. Ans. (b) Urea, Creatinine, Phosphate, Calcium
and potassium cancer after therapy. Therefore, ypTNM should
[Ref: surgery sixer page 944] consider only viable tumor cells and not signs
of regressed tumor tissue such as scars, fibrotic
•• Please remember Calcium is low all others are areas, fibrotic nodules, granulation tissue, or
increased mucin lakes

Chapter 1  Introduction to Oncology


3. Ans. (c)  y 4. Ans. (a)  1% cetrimide
[Ref: Internet Sources] [Ref: Internet journals]
•• The use of preoperative adjuvant therapy is •• The routine use of cetrimide as a tumoricidal
becoming increasingly frequent for a number of irrigant in colorectal surgery.
tumors. •• Rectal irrigation with various agents including
•• Therefore, the pathologic classification after mercuric perchloride, povidone iodine and
preoperative therapy may not reflect the true Cetrimide has been shown to be effective in
anatomic extent of disease before treatment. reducing anastomotic recurrence following
•• To indicate that the clinical or pathologic anterior resection.
classification has been determined after •• Of these various agents, cetrimide is in routine
use in many hospitals.
Extra Mile
AJC Classification
 T1: Tumor limited to antral mucosa of infrastructure without bone erosion.
 T2: Tumor of superstructure with no bone destruction or in infrastructure with medial bony wall destruction
 T3: Tumor invades the skin of cheek, pterygoid muscle, orbit and anterior ethmoid
102  T4: Cribriform plate, sphenoid sinus, nasopharynx skull base, pterygoid plates and posterior ethmoid involvement
is present.
Ohngren’s Line

Fig. 10:  Ohngren’s Line (Imaging line)

 An imaginary line drawn between medial canthus and angle of mandible.


 A growth above this line – suprastructure has poor prognosis
Lederman’s Classification
New SARP Series TUMOR

Fig. 11:  Lederman’s Classification

 Two lines one passing through antrum floor and roof divides area into 3 parts:
zz Intrastructure
zz Mesostructure
zz Suprastructure
 Suprastructure tumors are more complicated.
Other Non Coding Sequences in Human Genome
„„ MicroRNA
„„ Long non coding RNA
„„ Transposons
„„ Centromere
„„ Telomere
16 „„ Promoter and enhancer regions
„„ Transposons or jumping genes

TUMOR PROGESSION
„„ Can be explained by Galapagos finches theory
„„ Subclones which have the capacity to overgrow other tumor cells arises from the tumor (SURVIVAL OF THE
FITTEST)
„„ These subclones are later replaced by still malignant subclones
„„ This feature render the tumor to become more aggressive over time – Tumor PROGRESSION

Hallmark of Malignancy
„„ Self-sufficiency of growth signals
„„ Insensitivity to growth inhibition
„„ Altered cellular metabolism
„„ Evasion of apoptosis
„„ Limitless replicative potential
„„ Sustained angiogenesis
„„ Ability of invasion and metastasis
„„ Evasion of host defenses
„„ Genomic Instability
Hallmark of malignancy is ANAPLASIA (Lack of differentiation)

Self-Sufficiency of Growth Signals


„„ Oncogene: Genes that promotes its own growth in an autonomous fashion
„„ Protooncogene: Unmutated counterparts of oncogene Fig. 2:  Protooncogene promotes
„„ Aberrations in signalling pathways can lead to the development of tumors cancer
„„ The major signalling pathways affected includes:
G protein coupled Receptor pathway, WNT signalling pathway, Notch, Hedgehog, JAK/STAT pathway, etc.
TABLE 1:  Protooncogenes and their associated tumors

Category Protooncogene Associated tumor


New SARP Series TUMOR

GROWTH FACTORS
PDGF -β PDGFB Astrocytoma
Fibroblast growth factor FGF3 Osteosarcoma, Breast carcinoma, Gastric
carcinoma
TGF -α TGFA Astrocytoma
HGF HGF Hepatocellular carcinoma, thyroid
malignancies
Contd...
Category Protooncogene Associated tumor
GROWTH FACTOR RECEPTORS
ERBB1 (EGFR) Pulmonary adenocarcinoma
EGF Receptor family ERBB2 (Her2) Breast carcinoma
Receptor for Kit ligand KIT GIST, Seminoma
ALK receptor ALK Adenocarcinoma of lung,
17
neuroblastoma,
FMS like tyrosine kinase 3 FLT3 Leukemia
Receptor for neurotrophic factors RET MEN 2A, 2B
Familial medullary thyroid carcinoma
PROTEINS INVOLVED IN SIGNAL TRANSDUCTION
KRAS Carcinoma colon, lung and pancreas
HRAS Renal and urinary bladder tumors
NRAS Melanoma, hematological malignancies
GTP binding proteins GNAQ Uveal melanoma
GNAS Pituitary adenoma
JAK/STAT pathway JAK2 Myeloproliferative disorders, ALL
Non receptor tyrosine kinase ABL CML, ALL
Notch pathway NOTCH 1 Leukemia, lymphoma, carcinoma breast
NUCLEAR REGULATORY PROTEINS
Transcriptional activators C- MYC Burkitt lymphoma
N- MYC Neuroblastoma
CELL CYCLE REGULATORS
Cyclins Cyclin D1 Mantle cell lymphoma, Multiple
myeloma, Esophageal carcinoma, Breast
carcinoma

Chapter 2  Pathogenesis of Neoplasia


Cyclin dependent kinase CDK4 Glioblastoma, sarcoma, Melanoma

H igh Y ield fact


 All growth factors are protooncogenes except TGF – β which is a tumor suppressor gene

„„ Hepatocyte Growth Factor (HGF): HGF (Also called scatter factor), Receptor for HGF – MET

Extra Mile
Tumors Associated with BRAF Mutation
 Papillary thyroid carcinoma
 Malignant melanoma
 Colonic carcinoma
 Langerhan cell histiocytosis
 Hairy cell leukemia
AIIMS New Pattern 2019 Model Questions
1. Match the following C. BRCA1 gene is located on chromosome 17q21
A. APC - 1. Cowden Syndrome D. BRCA 2 gene is located on chromosome 13q12.3
26 B. PTEN - 2. Gastric carcinoma a. Option A and C are false
C. E Cadherin - 3. Familial Adenomatous polyposis b. Option B and C are true
D. PTCH - 4. Pancreatic carcinoma c. Option B is false
     - 5 . Peutz Jeghers syndrome d. Option A, B, C and D are true
- 6 . Basal cell carcinoma
a. A-3, B-2, C-1, D-6 Ans. (d)  Option A, B, C and D are true
b. A-3, B-6, C-1, D-4 Molecular classification of breast carcinoma:
c. A-3, B-1, C-2, D-6
d. A-3, B-5, C-6, D-4 Luminal A Luminal B Her 2 Triple
positive negative
Ans. (c)  A-3, B-1, C-2, D-6 ER +ve ER +ve ER -ve ER -ve
PR +/- PR +/- PR -ve PR -ve
2. Assertion: Rb gene is active in hyperphosphorylated Her 2 neu Her 2 neu Her 2 neu Her 2 neu
state -ve +ve +ve -ve
Reason: In hyperphosphorylated state, Her 2 neu
a. If both assertion and reason are true and the - ve (few
reason is the correct explanation of the Assertion cases)
b. If both assertion and reason are true but the
reason is not the correct explanation of the E.g: Tubular E.g: E.g:
Assertion carcinoma, Apocrine Medullary
c. If Assertion is true but reason is false mucinous carcinoma carcinoma
d. If Assertion is false and reason is true carcinoma Adenoid
Ans. (d)  If Assertion is false and reason is true cystic
•• Rb gene is active in hypophosphorylated state
carinoma
•• Rb gene is inactive in hyperphosphorylated state
4. 30 year old female was diagnosed to have breast
•• Hypophosphorylated Rb , complexes with E2F
cancer and was under treatment. During followup,
transcription factor and inhibits the transcription
she developed a lesion in the thigh measuring
of genes required for the Synthetic (S) phase of
8x8cm. Biopsy proved it to be a high grade sarcoma.
cell cycle.
3 months later, the patient developed headache
•• Phosphorylation of Rb gene by Cyclin dependent
and vomiting. CT brain was done and was found
kinases CDK4/cyclin D, CDK6/cyclin D
to have a brain tumor. Mutation in which of the
and CDK2/Cyclin E leads to release of E2F
(Elongation factor 2), thus leading to progression following gene could have been implicated in the
of S (Synthetic) phase causation?
a. APC
New SARP Series TUMOR

3. 40 year old nulliparous lady with family history


of breast cancer presented with lump in the upper b. PTEN
outer quadrant of right breast since 5 months. c. PTCH
Histopathology was reported as Invasive ductal d. p53
carcinoma, grade II. Choose the correct options e. WT-1
amongst the following
Ans. (d)  p53
A. BRCA 1 associated breast cancers are poorly The given history is in favour of Li-Fraumeni
differentiated syndrome which is due to mutation in p53 gene
B. Apocrine carcinoma is usually Her2 positive
5. Arrange the following in the sequence of Ans. (c)  CADB
occurrence in the causation of colonic carcinoma? Sequential arrangement of Model for colorectal
A. Activation of RAS carcinoma through adenoma-carcinoma sequence.
B. Loss of tP53 •• Inactivation of APC gene
C. Inactivation of APC gene •• Activation of RAS
D. Loss of tumor suppressor gene on 18q Loss of tumor suppressor gene on 18q
a. BACD b. BADC •• Loss of tP53
c. CADB d. ACBD 27

6. 56 year old farmer presented with pearly white lesion with telangiectasia on the face. Gross and microscopic
picture of a malignant neoplasm is given below. Identify the syndrome associated with the shown malignant
neoplasm.
a. Gorlin syndrome
b. Gardner syndrome
c. Wilms tumor
d. Tuberous sclerosis

Ans. (a)  Gorlin syndrome Chapter 2  Pathogenesis of Neoplasia


•• The given image shows basal cell carcinoma.
•• Histologically basal cell carcinoma shows peripheral palisading, retraction clefts and mucin deposition in the
stroma.
•• Gorlin syndrome is due to mutation in PTCH gene.
STAGES OF HEMATOPOIESIS
Hematopoiesis takes place in the following organs during development
„„ Till 3rd week – Yolk sac (Mesoblastic stage)
„„ 3rd Month – Liver (Hepatic stage)
„„ 4th month – Bone marrow (Myeloid stage)
Birth – Bone marrow
40 „„
„„ Adult – Bones in which red marrow is present – Vertebra, ribs, skull, sternum, pelvis, proximal epiphysis of humerus
and femur
„„ In Severe anaemia, EXTRAMEDULLARY Hematopoiesis can occur in liver and spleen.
„„ First definitive Hematopoiesis – Mesoderm of intraembryonic aorta, gonad and mesonephros(AGM)

Hematopoiesis At A Glance
New SARP Series TUMOR

Fig. 1:  Hematopoiesis at a glance


STRUCTURE OF A LYMPH NODE

41

Fig. 2:  Structure of a lymph node

Must Know
Most Common
 Most common haematological malignancy in children ALL
 Most common leukemia in adults CLL
 Most common site of extranodal lymphoma: Stomach
 Most common site of extranodal lymphoma in HIV patients: Central nervous system (CNS)
Origin of Lymphoma
 Burkitt lymphoma, Follicular lymphoma: Germinal center B cell
 Mantle cell lymphoma: Naive B cell
 Hairy cell leukemia, extranodal marginal zone lymphoma: Memory B cell
IHC Markers
 CD 3: Pan T cell marker
CD 19: Pan B cell marker

Chapter 4  Hemato-oncology

 CD 16, CD 56: NK cell marker
 CD13, 33: Marker for macrophages
 CD 34: Hematopoeitic stem cell marker
 CD 68: Histiocytic marker
 CD 38, CD138: Plasma cell marker
Translocations
 Burkitt lymphoma: t(8:14)
 Follicular lymphoma: t(14:18)
 Mantle zone lymphoma: t(11:14)
 Marginal zone lymphoma: t(11:18)
Special Stains
 Lymphoblasts: PAS and Tdt
 Myeloblasts: MPO, Sudan black
 TRAP: Hairy cell leukemia, Splenic marginal zone lymphoma
L atest U pdate
Macrophage/Dendritic Cell Neoplasm
Includes
 Langerhans-related histiocytosis
 Cutaneous and mucocutaneous histiocytosis
59
 Mallignant histiocytoses
 Rosai-Dorfman disease
 Hemophagocytic lymphohistiocytosis and macrophage activation syndrome

Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome


 Life threatening disease due to dysregulation of T cells.
 There is increased cytokines, leading to macrophage hyperplasia and increased phagocytosis
Clinical Features
 Fever, hepatosplenomegaly
 Lymphadenopathy, rashes
 Neurological features
 Hypertriglyceridemia, increased ferritin
 Coagulation abnormalities

Diagnostic Criteria
 Fever >35deg for more than 7 days
 Splenomegaly
 Cytopenia- Hb<9g/dl, PLT<100000cells/microl
 Increased triglycerides >2nmol/L, Hypofibrinogenemia<150mg/dl.
 Haemophagocytosis in bone marrow/spleen/lymph node.
zz Decreased/ absent NK activity
zz S. Ferritin > 500microg/L
zz Soluble CD 25> 2400 U/ml
5 major/ 4 major +A/ 4 major +A&B
Langerhans Cell Histiocytosis
 Langerhans cells have vesicular nuclei with grooves, and abundant vacuolated cytoplasm
Types
1. Multifocal multisystem Langerhans cell histiocytosis (Letterer Siwe disease):
zz Usually affects adults

Chapter 4  Hemato-oncology
zz Presents as seborrhoeic eruptions
2. Unifocal and multifocal unisystem Langerhans cell histiocytosis (Eosinophilic granuloma):
zz Unifocal lesions affects older children or adults
zz Multifocal unisystem affects young children

Must Know
Hand Schuller Christian Triad
Triad of:
Calvarial bone defects

Triad of

Diabetes insipidus Exophthalmos


VISUAL TREAT
1. Faggot cell: myeloblast with multiple auer rod 4. Flower cells – in adult t cell leukemia

61

2. 
Ringed sideroblasts: highlighted by prussian 5. Sezary cell – in sezary syndrome
blue stain

Chapter 4  Hemato-oncology
3. Chronic myeloid leukemia 6. Multiple myeloma


7. Mott cell 9. Hairy cell leukemia

62

8. CLL 10. Leucoerythroblastic blood picture


New SARP Series TUMOR
„„ Most common metastatic sites of prostate carcinoma are lymph nodes & bones
„„ Lymphatic metastasis occurs most commonly to → obturator lymph nodes
„„ Most common bony metastasis occurs in (in decreasing order)
zz Lumbar spine (most common)
zz Proximal femur
zz Pelvis
zz Thoracic spine
210 zz Ribs

Tumor Markers in CA Prostate


„„ Serum acid phosphatase is a tumor marker of prostate Ca.
„„ But now serum acid phosphatase assay has been superseded by PSA assay (prostate specific antigen)

Recent Advances
Prostate specific antigen
 It is a glycoprotein produced only in the prostatic cells (both benign & malignant). It facilitates liquefaction of
semen.
 It is neither sensitive nor specific for early prostate carcinoma, nevertheless it gives some help in making a diagnosis
zz Normal serum level  less than 4ng/ml.
zz Men aged 50-69 years: Level > 3-4 ng/ml; Advised Biopsy**
zz Localised cancers will have PSA < 10-15 ng/ml
zz Metastatic cancer will have PSA level > 30 ng/ ml
 Since PSA is not specific for Cancer- PSA velocity & PSA density are used to detect prostate cancer**

Staging of prostate cancer


 Tis → Carcinoma in situ
 T1 → These are incidentally found tumors in a clinically benign gland after TURP
zz T1a- <5% tumor in the resected specimen
zz T1b- >5% tumor in resected specimen
zz T1c- Detected due to elevated PSA level
 T2 → Tumor palpable by DRE or visible by TRUS, confined to capsule*
zz T2a- Tumor confined to one lobe
zz T2b- Tumor involving both lobe
 T3 → Extra capsular extension with or without seminal vesicle involvement
 T4 → Tumor directly extends into bladder neck, sphincter, rectum, pelvic side walls etc.
zz T1&T2 are early disease
zz T3&T4 are advanced disease
New SARP Series TUMOR

Fig. 5:  Staging of prostate cancer


ANATOMY OF SKIN
The skin is divided into two main layers:
„„ Surface epithelium (epidermis)
„„ Dermis
TABLE 1:  Structural or organization of skin
278 Epidermis Dermis
Keratinized stratified squamous epithelium contains following layers: Made up of two layers:
• Stratum Basale (deepest layer) • Superficial papillary
• Stratum Spinosum (Malpighian layer, Prickle cell layer) • Deep reticular layer
• Stratum Granulosum
• Stratum Lucidum
• Stratum corneum (Superficial layer)
„„ Melanocytes are found in the junction between Stratum Basal layer and Dermis
„„ Dermis is relatively avascular but contains tissue macrophages and mast cells.
„„ Melanin is transferred to the surrounding basal cells through dendritic process
„„ No of Melanocytes/unit area is same in all races

Fig. 1:  Layers of skin

ACQUIRED MELANOCYTIC NEVI


It is classified based on location of Nevus:
„„ Junctional: Between Epidermis (Stratum Basale and Dermis junction)
New SARP Series TUMOR

„„ Compound: Between Epidermis and partly into dermis


„„ Dermal: seen in the dermis itself.
Junctional Nevi is common in Children and has malignant potential in adult.

ETIOLOGY OF SKIN CANCERS


Actinic Damage: (SCC > BCC)
„„ Major Carcinogenic factor
„„ 90% if skin malignancies in sun exposed areas
„„ People at risk- Blue eyed, Fair skin, Blond and red hair
„„ Ultraviolet B in sunlight is highly carcinogenic.
„„ Ultraviolet light C in Arc welders is also carcinogenic.

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