Lymphoma

Lymphoma Origins (B-cell Pathway)

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Mnemonic:
  • Hair - memory
  • Margin - margin
  • mantle - mantle
  • post germ → Post PG → HOD
  • Naive → Calling (CLL) Naive
  • Germ → germ in a flower (Follicular) → nokki Bark (Burkitt) cheyth

Hodgkin's Lymphoma (HL)

PATHOGENESIS

  • Epstein-Barr Virus (EBV)
  • Latent membrane protein 1 (LMP-1) virulence factor
  • Increased activation of NF-κB growth signalling pathway
  • Post-germinal B cell proliferation
  • Hodgkin's lymphoma

Ivory vertebrae.

  • Seen in
    • Pagets disaese
    • Hodgkins Lymphoma
    • Blastic mets
      • Breast Ca
      • Prostate Ca
    • HOD Page il Ivory kuthi vach

Classical Hodgkin's Lymphoma:

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Lacunar - nodular
Lacunar - nodular
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Four Types:

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Nodular sclerosis
 ↳ folded or multilobed nucleus
 ↳ surrounded by open space
Nodular sclerosis
folded or multilobed nucleus
↳ surrounded by
open space
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  • HOD went on a CAR () to Anthra () Win (Vincristine) some Blow ()
HL
Features
Mnemonic:
Classical Hodgkins
CD15, CD30
PAX 5
• EBV positive (except Nodular)
Odd nos
(1, 3, 5)
↳ 1. Nodular Sclerosis
Most common worldwide. 
Lacunar RS cells 
• (whitish area around owl-eye).
Not associated with EBV
Nodular → World
has Lakhs (Lacunar) of money
No kissing (No EBV)
↳ 2. Mixed Cellularity
Most common in India.
• Assoc. EBV, HIV.
Classical RS cells.
Maximum associated with EBV
India → Mixed population → Sex and kiss (EBV, HIV) → Classical movies (Classical RS cells)
↳ 3. Lymphocyte Rich
Mononuclear RS cells 
(one nucleus)
• Associated with EBV
Best Prognosis
Rich people roam around for money → finally they will be single
↳ 4. Lymphocyte Depleted
Mummified RS cells.
Assoc. immunodeficiency/HIV
Worst prognosis.
• Associated with EBV
Depleted → Dead → mummified → deadly disease (HIV)
Non Classical Hodgkins
CD20 +
CD45+
EMA +
BCL-6 +
EBV LMP -
POPCORN CELL
Even (EMA) nos

2, 4, 6, EMA
  • Associated with EBV.
  • Characterized by Reed-Sternberg (RS) cells (owl-eye).
    • Large, bi-nucleated cells with prominent nucleoli.
  • RS Cell Markers: CD15, CD30, PAX5.
    • CD30: Most sensitive.
    • PAX5: Most specific.

Clinical Presentation

  • Average age group: Middle-aged - elderly.
  • B symptoms:
    • Fever: 
      • For >10 days.
      • Pel Ebstein type (waxing & waning pattern).
    • Night sweats.
    • Weight loss.
  • Generalized/cervical lymphadenopathy.
    • Painless
    • Rubbery
    • Most commonly affected lymph node: 
      • Cervical lymph node.
  • Hepatosplenomegaly in 30%
  • SVC syndrome due to obstruction from mediastinal LN involvement
      • Mediastinal involvement differential diagnosis (D/D):
        • T ALL
        • Nodular Sclerosis → Hodgkin Lymphoma
        • Thymoma
  • Paraneoplastic syndromes:
    • Amyloidosis: 
      • AA type.
    • Pain with alcohol ingestion.
    • Intense pruritis.

Nodular Sclerosis:

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Non-Classical Hodgkin's Lymphoma (NLPHL):

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  • aka Nodular Lymphocyte Predominant Hodgkin Lymphoma (NLPHL).
  • Has maximum B symptoms
  • Not associated with EBV, CD15, CD30.
  • Markers: CD20+, CD45+, EMA (epithelial membrane antigen)+, BCL6+.
  • Shows popcorn RS cells (convoluted).
  • Best prognosis overall.
    • Nodular types often good prognosis
      • Mnemonic: NLPHL (popcorn) = best.
  • Mnemonic: 20 (CD20) vayassula Ima (EMA), 45 (CD45) vayassulla alde, backil (BCL2) adichu, for popcorn ()

MANAGEMENT

Treatment:

  • ABVD regimen:
    • A - Adriamycin (Doxorubicin).
    • B - Bleomycin.
    • V -Vinblastine.
    • D - Dacarbazine.

Ann Arbor staging system:

Stage
Description
Stage 1
Single Lymph Node (LN) region or single extralymphatic organ involvement.
Stage 2
Two or more LNs on same side of diaphragm.
Stage 3
Both sides of diaphragm involved.
Stage 4
Multiple/disseminated foci involved with one or more extralymphatic organs.

Prognostic Factors: 

  • Staging > tumour type.

Note: 

  • Hairy cells exhibit markers: Annexin A+, CD 25+, CD 11c+, CD 103+.

Myeloproliferative disorders

  • Group of disorders with increased production of:
    • Red blood cells
    • White blood cells
    • Platelets
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WHO Classification

  • Chronic myeloid leukemia (CML)
  • Polycythemia vera (PV)
  • Primary myelofibrosis (PMF)
  • Essential thrombocythemia
  • Juvenile myelomonocytic leukemia (JMML)
  • Chronic neutrophilic leukemia (CNL)
  • Chronic eosinophilic leukemia
  • Myeloproliferative neoplasm, not otherwise specified (MPN-NOS)
  • Note - CLL not included
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Feature
Hodgkin's Lymphoma (HL)
Non-Hodgkin's Lymphoma (NHL)
Age Group
Bimodal peak:
Elderly
• 15-20 yrs
• Elderly
LN Spread
Contiguous (e.g., cervical → supraclavicular → axillary nodes)
Non-contiguous
Much less predictable
Spread involvement (neck & spleen)
Lymph Node (LN) Involvement
Single axial group of nodes (Cervical and mediastinal)
Multiple peripheral nodes
Painless, non-tender, 'rubbery' superficial lymph nodes
Painless, slowly progressive peripheral lymphadenopathy (most common)
Extranodal Involvement
Less common (L/c)
More common (M/c)
Mesenteric Involvement
L/c
M/c
Waldeyer's Ring Involvement
L/c
M/c
Microscopy
Reed-Sternberg cells present
Reed-Sternberg cells rare or absent
Inflammatory background (lymphocytes, eosinophils etc.)
No inflammatory background
Constitutional (B) Symptoms
Present
(fever, night sweats, weight loss)
Less common at presentation
Indicates disseminated disease
Common in advanced/end-stage disease
Other Organ Involvement
SPLENOMEGALY IN 30%
Hepatosplenomegaly
SVC syndrome due to obstruction from mediastinal LN involvement
Bone marrow frequently involved
May be associated with pancytopenia
Note
Lymph node excision biopsy to diagnose
Most derived from B-cell lines
Known as HIV-related lymphoma

Non-Hodgkin's Lymphoma (NHL)

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Two types:

  1. B-NHL (7 types)
  1. T-NHL (2 types).

Genetics Summary

Translocations

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CD Markers Summary:

Dumb Brat → Shows off
Dumb Brat → Shows off

BNHLs (7 Types):

BNHLs
Features
Mnemonic
1. Follicular Lymphoma
Best prognosis
“waxing and waning” LN
• T(14;18).
CD 10 +
BCL 2 + (anti-apoptotic)
Escape apoptosis
↑ Cell Proliferation
Mnemonic: Teenagers 14 & 18 →friendly, best prognosis

10th std (CD10) → back seat 2 guys friends (BCL2)
2. DLBCL
Worst prognosis.
Most common NHL.
3. Burkitt's Lymphoma
4. CLL/SLL
CD5+, CD23+, CD200+
DELETION 13q
Mnemonic: "subkuch positive"
5. Mantle Cell Lymphoma
CD5 positive
CYCLIN D1+
SOX 11+

Cleaved/buttock cells
Lymphomatoid polyposis

• t(11;14)
Teenager with younger = mental, mad

5 year old likes hanging out with 11 and 14 (t11:14) year olds → and go mental (Mantle) → Cycle (Cyclin D1) il Socks (SOX11) itt pokum
6. Marginal Zone Lymphoma/ MALTOMAS
Everything negative

• t(11;18)
Margins of 11 → 14 → 18

Ignore/neglect the margin
7. Hairy Cell Leukemia

3. Burkitt's Lymphoma:

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  • Vacuolations → seen in
    • Burkitt’s Lymphoma
    • ALL L3 (Oil red O)
    • notion image
  • Classical: African child, jaw swelling.
  • Chr 8 + Even No. 
    • 8;14, 8;22, 2;8
    • Mnemonic: 8 looks like B → Chromosome 8
    • NOTE: Translocation 8;21 → AML M2
  • Associated with
    • C myc,
    • Ki 67 100%
    • EBV.
  • M/c NHL, M/c aggressive, M/c extranodal
  • Cells: Cytoplasmic vacuolations, Oil Red O positive (fat).
  • Biopsy: "Starry sky appearance" (white macrophages vs dark blue tumor).
    • notion image
  • Mnemonic: Bar il poi → Pcket kaliyayi (vacuolation), Mike vach pattu padi (C myc), Jaw yil (Jaw swelling) Kiss (Ki67) cheyth (→ EBV) → Star nokki kidannu

7. Hairy Cell Leukemia:

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  • Common in: Boys.
  • Mutation: BRAF mutation.
  • Presentation
    • Hypercellular Pancytopenia
  • Markers: 
    • Annexin A1+
    • TRAP+ (red color) 
    • DBA 44+ (new)
  • Old Markers: 
    • CD11, CD25, CD103 (CD103 important, side profile).
  • Microscopy:
    • Best on face contrast microscopy.
  • Splenomegaly:
    • Affects red pulp of spleen.
  • Infections:
    • Often MAC (Mycobacterium Avium Complex) due to pancytopenia.
  • Bone Marrow:
    • Aspirate = dry tap.
    • Biopsy = "fried egg appearance".
  • Mnemonic of Hairy Cell Leukemia:
    • Boys (mc) have red hair (HCL) (TRAP+ → red color; Spleen red pulp)
    • He is dumb (DBA 44) and Brat (BRAF)
    • Only eat eggs (fried egg on BMB)
    • Use MAC (Mycobacterium avium complex) to show off
    • He brought a useless tap (dry tap) for 103 Rs (CD103) instead of buying for 11 (CD11) or 25 () Rs.
      • Mnemonic: 103 → face turned to side (refer screenshot)
    • So Trapped (TRAP) cheyth face (Face contrast) idich Red Pulp (Spleen red pulp) aaki
  • Cladribine: 
    • DOC for Hairy cell Leukamia
    • Mnemonic: Clara → hairy
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  • Cladribine, Pentostatin
    • ⛔ ADA
    • NOTE: SCID
      • ADA deficiency
  • Lesch Neyhan syndrome
    • ⛔ HGPRT

TNHLs (2 Types):

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Anaplastic Large Cell Lymphoma (ALCL):

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  • CD30 positive.
  • Shows 
    • donut cells
    • hallmark cells (kidney-shaped)
  • Mnemonic:
    • Anaplastic → ANayude Kidney eduth vaishna donut undakki 30 Rs nu vittu
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Granuloma Shapes

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NOTE: donut cellsAnaplastic Large Cell LymphomaCD30
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Mycosis Fungoides (MF)

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  • Paul (Pautriers) tried sex (sesary) with
    • mike (mycosis) → 45 yr old and
    • dani (denileukin) → 4 yr old
    • → Into brain (cerebriform nucleus)
  • Description:
    • Cutaneous T-cell lymphoma (CTCL) variant
    • T-cell tumour in skin
  • Cell Proliferation:
    • CD4 positive &
    • CD45 RO positive helper T-cells
  • Course: Very indolent
  • Metastasis: Very commonly seen
  • Skin biopsy: 
    • Pautrier's microabscesses (cancer cell clusters).
      • Mnemonic: PM → MP (Pautrier's for Mycosis, Munro's for Psoriasis).
        Mnemonic: PM → MP (Pautrier's for Mycosis, Munro's for Psoriasis).
  • Blood spread → Sézary Syndrome.
    • Sézary cells with cerebriform nuclei (brain-like).
  • DNA analysis
    • Clonal arrangement of T cell receptor genes (TCR gene)Standard now
    • Mycoides → Fungal → Flower like
    • Fungoides → T cell cancer ⇒ Clonal arrangement of TCR

Clinical Presentation:

  • Location:
    • Trunk (central girdle),
    • upper lower limb
    • Central body
  • Stages:
    • Patches,
    • plaques,
    • tumour/nodular,
    • erythroderma

Sezary Syndrome:

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Triad

  1. Erythroderma
  1. Peripheral lymphadenopathy
  1. Sezary cells (>20% lymphocyte count OR >1000 cells/mm³)
      • Atypical lymphocytes
      • Grooved or cerebriform nucleus
      • Seen in tissue & blood
      • Mnemonic: Sezary cell → Sezary seed → middle groove (+)
  • Cerebriform appearance
    • Inverted papilloma → Thala (Cerebriform) thirinjavan

Histopathology:

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  • Epidermotropism:
    • Many T-lymphocytes in epidermis
  • Pautrier's microabscesses:
    • Collections of T-cells forming microabscesses in epidermis
    • Poultry → easily infected with fungus → fungoides
      • notion image

Treatment:

  • Total Skin Electron Beam Therapy (treatment of choice)

Newer Drug:

  • Denileukin Diftitox (IL2 fusion toxin)
  • Mnemonic: Di → Di → 2

Multiple Myeloma (MM)

  • Mulburry Mottu () Russel () and dutcher () put in flame ()
  • Lena (Lenalidomide) boatil (Bortezomib) 10 days (Dexamethasone) Tharattupadi (Daratumumab)

SKULL XRAY PATTERN APPROACH

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  • Definition: Cancer of plasma cells.

Normal Plasma Cell:

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  • Eccentric nucleus.
  • Cartwheel chromatin.
  • Perinuclear halo (Golgi for antibody synthesis).
  • vs. Osteoblast:
    • Also eccentric nucleus but paranuclear halo (shuttlecock appearance).
      • notion image

Diagnostic Criteria (CRAB & SLIM):

  • Bone marrow plasma cells > 10%.
  • Immunoglobulin (Ig) level > 3 g/dL (most common IgG).

Myeloma Defining Events:

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  • CRAB SLM
    • C: Calcium elevated.
    • R: Renal insufficiency.
    • A: Anemia.
    • B: Bony lytic lesions (X-ray: skull, vertebra; MRI: focus > 5mm).
    • S: Sixty 60% plasma cells in bone marrow.
    • L: Light chain ratio abnormality.
    • M: MRI focal lesions > 5 mm.
  • New IMWG biomarkers (≥60% cells, FLC ratio ≥100, MRI lesions)
    • → diagnosis even without CRAB.
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  • MGUS
    • Monoclonal gammopathy of Undetermined significance
    • premalignant;
  • Smoldering
    • intermediate.

NOTE: β 2

  • Microglobulin Multiple Myeloma, Dialysis
  • Transferrin CSF
  • Glyocoprotein APLA

Peripheral Smear

  • Plasma cells usually not seen.
  • Rouleaux formation of RBCs.
    • notion image

Bone Marrow Aspirate Inclusions 
(all are immunoglobulins, mostly IgG):

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Russell bodies: Intracytoplasmic.
Russell bodiesIntracytoplasmic.
Dutcher bodies: Intranuclear.
Dutcher bodies: Intranuclear.
  • Mott cell/Mulberry cell
  • Flame cells:
    • Look "on fire"
    • M/c with IgA increase.

Bone Marrow Biopsy: 

  • Sheets of plasma cells 
    (eccentric nuclei).

Electrophoresis (Serum): 

  • M-spike in gamma region
    (myeloma/monoclonal spike,most commonly IgG, don't confuse with IgM).
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  • Mulburry Mottu () Russel () and dutcher () put in flame ()
  • Lena (Lenalidomide) boatil (Bortezomib) 10 days (Dexamethasone) Tharattupadi (Daratumumab)

Punched out lytic lesion/ rain drop lesion

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  • Well defined lytic lesions in the skull.
  • Involves outer and inner tables equally.
  • Seen in multiple myeloma & LCH
  • It is a lytic lesion:
    • No new bone formation.
    • No increase in ALP.
    • No hot spots on bone scan.

Plasma Cell Leukemia: 

  • > 20% plasma cells in peripheral blood.
  • Myleoma → > 20% plasma cells in bone marrow
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  • CD Markers for Plasma Cells:
    • Plasma Cell Type
      CD45 (WBC marker)
      CD19 (B cell marker)
      CD38
      CD138
      Normal Plasma Cell
      +
      +
      +
      +
      Malignant (MM)
      -
      -
      +
      +
      Multiple myeloma → bad kid → do not show markers of Parents (WBC and B cell)
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