Radiation Beyond Indication
Dr Kanhu Charan Patro
MD,DNB(Radiation Oncology),MBA,FICRO,FAROI(USA),PDCR,CEPC
Clinical Director, HOD-Radiation Oncology
ISRo- Institute of Stereotactic Radiation oncology
Mahatma Gandhi Cancer Hospital & Research Institute, Visakhapatnam
drkcpatro@gmail.com /M- +91-9160470564/ www.drkanhupatro.com
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Remember this slide
• There is a role of Radiation in benign diseases
• Many sites are under explored
• Practice with caution
• Mostly indicated in refractory/recurrent cases
• Practice with caution in young population
• Follow guideline
• More awareness required
• Do not forget about radiation induced malignancy
DEGRO Guidelines – Radiotherapy of Non-
Malignant Disorders (Part I)
DEGRO Guidelines – Radiotherapy of Painful
Degenerative Skeletal Disorders (Part II)
DEGRO Guidelines – Radiotherapy of Non-
Malignant Hyperproliferative Disorders (Part III)
Radiotherapy for Non-Malignant Symptomatic Functional Disorders
(Heterotopic Ossification & Graves Orbitopathy) (Part IV)
1. Anti-inflammatory Effects
• Low-dose radiation reduces inflammatory cell
migration
• Inhibits adhesion molecules (ICAM-1, E-selectin)
• ↓ Pro-inflammatory cytokines (TNF-α, IL-1, IL-6)
• ↑ Anti-inflammatory cytokines (TGF-β1, IL-10)
• Useful in arthritis, bursitis, fasciitis
2. Immune Modulation
• Alters macrophage polarization (M1 → M2)
• Reduces nitric oxide and oxidative burst
• Prevents chronic tissue damage
• Restores tissue homeostasis
3. Analgesic (Pain-Relieving) Pathways
• Indirect effect via ↓ inflammation
• ↓ Pain mediators (substance P, bradykinin)
• Reduces edema and vascular permeability
• Helps in degenerative skeletal disorders
4. Anti-proliferative Effects
• Inhibits fibroblast proliferation
• Reduces collagen deposition
• Prevents abnormal tissue growth
• Applied in keloids, heterotopic ossification,
Graves’ orbitopathy
5. Vascular and Tissue Remodeling
• Endothelial apoptosis at higher doses
• Low-dose stabilizes vascular function
• ↓ Leukocyte adhesion, permeability
• Contributes to healing and reduced swelling
6. Long-Term Adaptation
• Balance of benefit vs. late toxicity
• Benign disease uses low total doses
• Risk of late carcinogenesis is minimal
• Effective for chronic conditions with high
safety margin
Radiobiological Mechanisms
• Dose–response:
• ≥2 Gy: pro-inflammatory
• <1 Gy: anti-inflammatory (LD-RT)
• Effects at ~0.5 Gy:
– ↓ Leukocyte adhesion to endothelium
– ↑ TGF-β1 (anti-inflammatory cytokine)
– Apoptosis of PBMC, PMN → ↓ inflammation
– ↓ iNOS, ROS, NO → reduced edema, pain
– ↓ NF-κB, IL-1; ↑ TGF-β1
Preclinical Evidence
• Animal arthritis models confirm benefits:
• Reduced cartilage/bone destruction
• Improved joint swelling & pain
• Inhibition of IL-1, iNOS
• Upregulation of protective proteins (Hsp70,
HO-1)
• Optimal at 0.5 Gy fractions
Radiogenic Risk
• Effective dose (Sv): weighted organ/tissue
doses
• Cancer risk: ~5.5% per Sv (ICRP 2007)
• Genetic risk: negligible in LD-RT
• DDREF: ICRP=2 (<0.2 Sv), German SSK=1
• Example: Knee RT 6×0.5 Gy → ~0.1% added
cancer risk
• Higher risk in younger patients
Key Takeaways
• Benign RT uses same principles as cancer RT
• LD-RT (≤1 Gy/fraction) → strong anti-
inflammatory effects
• Clinical benefit proven, esp. at 0.5 Gy
• Radiogenic risks must be weighed, esp. in
young patients
• More epidemiological data needed
Shoulder Syndrome
Shoulder Syndrome
• Painful periarthritis of shoulder joint.
• Response rates: 58–100% (CR+PR).
• Large series (7,928 pts):
– CR 55%,
– PR 33%,
– Non-responders 12%.
• Better outcomes with early RT (<6 months pain).
• Technique: Opposing fields (LINAC 6 MV) or orthovoltage.
• Dose: 0.5–1 Gy/fx, 3–6 Gy total, 2–3 fx/week.
• LoE 4, GR C.
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Shoulder Syndrome
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Shoulder Syndrome
Elbow Syndrome (Epicondylitis)
Elbow Syndrome (Epicondylitis)
• Painful degenerative enthesiopathy at epicondyles.
• Evidence: >2000 pts, ~82% pain relief.
• CR 45%, PR 35%.
• Dose trials: 1 Gy/fx superior to very low dose.
• Technique: Orthovoltage single field or LINAC
fields/electrons.
• Dose: 0.5–1 Gy/fx, 3–6 Gy total.
• LoE 2c, GR B.
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Elbow Syndrome (Epicondylitis)
Elbow Syndrome (Epicondylitis)
Trochanteric Bursitis
Trochanteric Bursitis
• Inflammation/degeneration of trochanteric bursae.
• Results: 73% response (CR 23–38%, PR 18–50%).
• Technique: Include bursae (gluteus maximus
region).
• LINAC: opposing fields (6–10 MV).
• Dose: 0.5–1 Gy/fx, 3–6 Gy total.
• LoE 4, GR C.
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Trochanteric Bursitis
Trochanteric Bursitis
Plantar Fasciitis (Heel Spur)
Plantar Fasciitis (Heel Spur)
• Painful enthesiopathy at heel insertion.
• Response: CR 12–81%, PR 7–74%.
• RCTs: 0.5 Gy x 6 vs 1 Gy x 6 → both effective.
• Technique: Orthovoltage with bolus;
• LINAC 4–6 MV opposing fields.
• Dose: 0.5–1 Gy/fx, 3–6 Gy total.
• LoE 1b, GR A.
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Plantar Fasciitis (Heel Spur)
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• Plantar fasciitis
– It is an inflammation or degeneration of the plantar fascia, the thick band of tissue that connects your
heel to your toes.
– The main symptom is heel pain, especially worse with the first steps in the morning or after long periods
of rest.
– It happens because of overuse, strain, or micro-tears in the fascia.
• Calcaneal spur
– It is a bony outgrowth (osteophyte) from the calcaneus (heel bone).
– It often forms where the plantar fascia attaches to the heel.
– Many people with a calcaneal spur do not have pain. Sometimes it is just an incidental finding on X-ray.
• Relationship between the two
– Plantar fasciitis can lead to the formation of a calcaneal spur because of chronic traction at the heel
attachment site.
– But a spur is not necessary for plantar fasciitis. You can have plantar fasciitis without a spur, and you can
have a spur without pain.
– Heel pain is usually due to plantar fasciitis itself, not the spur.
• 👉 In short: Plantar fasciitis is a soft-tissue problem; calcaneal spur is a bone change. They
are different conditions, but they often coexist.
Plantar Fasciitis (Heel Spur)
Osteoarthritis Knee
Osteoarthritis Knee
• Degenerative disease of knee joint.
• Response rates: 58–91% (10,000+ pts).
• Technique: Include cartilage, bone, synovia,
muscles.
• LINAC: opposed ventro-dorsal or lateral fields.
• Dose: 0.5–1 Gy/fx, 3–6 Gy total.
• LoE 2c, GR B.
Osteoarthritis Knee
Osteoarthritis Knee
Osteoarthritis HIP
Osteoarthritis HIP
• Degenerative hip joint disease.
• Response rates: 24–89% (895 pts).
• Technique: Include cartilage, bone, synovia,
muscles.
• LINAC: 2 opposed ventro-dorsal fields.
• Gonadal shielding advised.
• Dose: 0.5–1 Gy/fx, 3–6 Gy total.
• LoE 4, GR C.
Osteoarthritis HIP
Osteoarthritis HIP
Hand & Finger Joint Arthrosis
Hand & Finger Joint Arthrosis
• Degenerative arthritis of small joints.
• Response rates: 63–75% (809 pts).
• Technique: Cover cartilage, bone, synovia,
periarticular tissues.
• LINAC/Orthovoltage: dorsal or ventral field.
• Shield nails if possible.
• Dose: 0.5–1 Gy/fx, 3–6 Gy total.
• LoE 4, GR C.
Hand & Finger Joint Arthrosis
Hand & Finger Joint Arthrosis
Morbus Dupuytren
Morbus Dupuytren
• Palmar fascia → finger contractures
• Best results in early nodular stage
• Dose: 30 Gy (2 × 5 × 3 Gy, 12-wk gap)
• LoE: 2c; GR: B
• 67–84% long-term control
Morbus Dupuytren
Morbus Dupuytren
Morbus Ledderhose
Morbus Ledderhose
• Plantar aponeurosis involvement
• RT for progression or post-surgery
• Dose: 15–21 Gy in 5 fractions
• LoE: 4; GR: C
• Symptom relief/stabilization
Morbus Ledderhose
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Morbus Ledderhose
Keloids
Keloids
• Excessive scar tissue, high recurrence post-excision
• RT reduces recurrence: 60–80% → 10–30%
• Dose: 16–20 Gy in 5 fractions
• Start within 24h post-surgery
• LoE: 4; GR: C
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Keloids
Peyronie’s Disease
Peyronie’s Disease
• Plaques in tunica albuginea → penile curvature & pain
• RT effective in early/soft plaques
• Dose: 10–20 Gy (2–3 Gy fractions)
• LoE: 2c; GR: B
• Improves pain & plaque softening
Peyronie’s Disease
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Peyronie’s Disease
Desmoid Tumors
Desmoid Tumors
• Aggressive fibromatosis, high recurrence post-surgery
• RT improves local control
• Dose: 50–60 Gy (post-op); 60–65 Gy (primary/inoperable)
• LoE: 3; GR: C
• Effective in primary & recurrent disease
Desmoid Tumors
Desmoid Tumors
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Vertebral hemangioma
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Vertebral hemangioma
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Vertebral hemangioma
Pigmented Villonodular Synovitis
Pigmented Villonodular Synovitis
• Synovial proliferation, high recurrence post-surgery
• RT improves local control (~90–95%)
• Dose: 30–40 Gy, CT/MRI planning
• LoE: 2c; GR: B
Pigmented Villonodular Synovitis
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Pigmented Villonodular Synovitis
Gorham–Stout Syndrome
Gorham–Stout Syndrome
• Rare osteolysis (vanishing bone disease)
• RT controls progression in ~77%
• Dose: 36–45 Gy
• LoE: 2c; GR: B
Gorham–Stout Syndrome
Gorham–Stout Syndrome
Pterygium
Pterygium
Aspect Details
Indication
Recurrent pterygium after surgical excision; aggressive/vascular
pterygium with high recurrence risk
Timing Usually applied postoperatively within 24–48 hours of excision
Dose
Single fraction 5–10 Gy (commonly 7–8 Gy) to
scleral surface; or fractionated regimen e.g., 2
Gy × 5 fractions (total 10 Gy)
Technique
Surface application using strontium-90 (Sr-90) applicator or beta-plaque;
shields used to protect cornea and lens
Procedure
Local anesthesia, surgical excision of pterygium, immediate application
of beta-radiation probe to bare sclera for prescribed duration
Advantages Reduces recurrence rate significantly compared to surgery alone
Risks/
Complication
s
Scleral necrosis, cataract, keratitis, delayed epithelial healing (rare with
modern dosing)
Pterygium
Pterygium
ORBITAL PSEUDOTUMOR
ORBITAL PSEUDOTUMOR
Aspect Details
Indication
Refractory orbital pseudotumor (idiopathic orbital inflammation) not
responding to corticosteroids or immunosuppressants. Pain, proptosis,
vision-threatening inflammation.
Dose
Conventional: 20 Gy in 10 fractions (2
Gy/fraction).Alternative: 20–30 Gy in 10–15 fractions.Low-dose
regimens: 4–10 Gy in 2–5 fractions for palliation/recurrence.
Procedure
External beam radiotherapy (EBRT), typically with 6 MV
photons.Immobilization with thermoplastic mask.CT-based planning,
conformal fields/IMRT preferred to spare lens and optic nerve.Field:
orbit only, margin to cover inflammation.
Response
Symptom relief in 60–80% of cases (pain, edema, proptosis).Best results
in lymphoid-predominant histology; fibrotic type responds less.
Toxicity
Usually minimal with low doses. Possible late effects: cataract, dry eye,
retinopathy (rare at ≤20 Gy).
ORBITAL PSEUDOTUMOR
ORBITAL PSEUDOTUMOR
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Heterotopic Ossification (HO)
• Heterotopic ossification (HO) is a medical condition where bone grows in
soft tissues and muscles where it doesn't normally exist.
• It's a common complication after injuries, surgeries, or certain conditions
like spinal cord injuries and burns.
• HO can be asymptomatic, but more severe cases may cause decreased joint
motion, pain, and a palpable mass.
• Treatment often involves a combination of physical therapy, medications
like NSAIDs, and sometimes radiation or surgery to prevent or remove the
abnormal bone growth.
Heterotopic Ossification (HO)
• Timing: 4h pre-op to 72h post-op
• Dose options:
–Single fraction: 7–8 Gy
–Fractionated: 5 × 3.5 Gy
• Effect: reduces incidence from 90% →
<10%
• LoE 1–2; Grade A–B
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Heterotopic Ossification (HO)
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Heterotopic Ossification (HO)
Graves Orbitopathy (GO)
• Autoimmune, thyroid-associated orbital inflammation
• Risk factors: Graves’ disease, hyperthyroidism, smoking, genetics
• Clinical: exophthalmos, diplopia, optic nerve compression
• Classification: NOSPECS (0–VI), LEMO
GO – Radiotherapy
• Used in moderate active phase (NOSPECS II–V)
• Response rates: 65–75% good/excellent
• Best in early inflammatory phase
• Can combine with corticosteroids (superior to
steroids alone)
• Doses:
• • Low dose: 0.3–2 Gy/fx, total 2.4–16 Gy
• • Standard: 2 Gy × 8–10 fx, total 16–20 Gy
• LoE 2; Grade B
GO – Radiotherapy
GO – Radiotherapy
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Neurogenic excess Salivation- Ptyalism
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Neurogenic excess Salivation- Ptyalism
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Neurogenic excess Salivation- Ptyalism
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Kimura's disease
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Kimura's disease
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Kimura's disease
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DFSP
Dermatofibrosarcoma Protuberans
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DFSP
Dermatofibrosarcoma Protuberans
Setting Dose Margins/Technique Outcome
Post-op
(close/positive
margin)
60 Gy
Scar + 3–5 cm CTV,
IMRT/3DCRT
↓ Recurrence, ~85–
90% control
Gross/unresectable 66–70 Gy
Wide CTV, advanced
technique
(IMRT/VMAT)
Local control ~80%
Definitive (non-
surgical)
66–70 Gy
Conformal/IMRT,
cover tumor +
margin
Useful if surgery not
feasible
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DFSP
Dermatofibrosarcoma Protuberans
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DFSP
Dermatofibrosarcoma Protuberans
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Plantar wart
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Plantar wart
Aspect Details
Indication
Refractory plantar warts (painful, recurrent, resistant to topical, cryotherapy,
laser, or surgical treatment)
Rationale Radiation induces local immune modulation and destruction of HPV-infected
keratinocytes
Technique Superficial radiotherapy (SRT-100 or contact therapy), low-energy X-rays
Dose Typically 2–3 Gy per fraction, 4–5 fractions; total dose 8–15 Gy
(varies by protocol)
Procedure Outpatient; direct application with lead shielding to protect normal tissue
Efficacy High clearance rates (70–90% in small series) with durable control in many
patients
Toxicity
Usually mild—erythema, desquamation, transient tenderness; very low risk of
long-term complications with low-dose localized treatment
Limitations
Rarely used today due to concern for carcinogenesis, reserved for resistant or
painful lesions in adults
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Plantar wart
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Plantar wart
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Nasopharyngeal Angiofibroma
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Nasopharyngeal Angiofibroma
Aspect Details
Dose
Typically 30–36 Gy in 1.8–2 Gy
fractions; some series go up to 40–45
Gy for resistant disease
Technique
Conformal RT or IMRT preferred
(minimizes dose to optic structures,
pituitary, brainstem)
Fractionation Conventional fractionation (1.8–2 Gy
per fraction)
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Nasopharyngeal Angiofibroma
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Nasopharyngeal Angiofibroma
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Psoriatic arthritis
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Psoriatic arthritis
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Psoriatic arthritis
Aspect Details
Indication
Severe, refractory psoriatic arthritis not controlled with medical therapy (NSAIDs,
DMARDs, biologics). Used mainly for local joint pain and inflammation.
Mechanism Low-dose radiation exerts an anti-inflammatory and immunomodulatory effect,
reducing synovitis and joint pain.
Dose
Typically 0.5–1.0 Gy per fraction, delivered 2–3 times per week;
total dose 3–6 Gy per course. Sometimes repeated after 2–3
months if needed.
Technique
Orthovoltage or megavoltage radiotherapy. Treated joints (hands, knees, ankles, etc.)
are localized. Low-energy photons commonly used.
Efficacy Symptomatic relief (pain reduction, improved function) reported in 60–80% of
patients.
Toxicity
Minimal at these doses; mild skin erythema possible. Carcinogenic risk is very low at
such low doses but considered in young patients.
Current Use Rare in routine practice due to availability of biologics. Still used in Europe (especially
Germany) for benign inflammatory conditions.
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Psoriatic arthritis
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Rheumatoid arthritis
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Rheumatoid arthritis
Aspect Details
Indication Historically used for severe, refractory RA when other treatments failed. Now largely
abandoned due to effective disease-modifying anti-rheumatic drugs (DMARDs) and biologics.
Technique Low-dose external beam radiotherapy or intra-articular radionuclide synovectomy
(radioisotopes like Yttrium-90, Rhenium-186, Erbium-169).
Dose
- External beam: 0.5–1 Gy per fraction, total 3–6 Gy.- Radionuclide
synovectomy: isotope activity varies by joint size (e.g., Y-90 for large joints, Re-186 for
medium, Er-169 for small).
Procedure Outpatient; isotope injected intra-articularly under aseptic conditions, often with local
anesthesia. Immobilization for 48 hours post-injection.
Effect Anti-inflammatory effect, relief of pain and swelling, reduced synovial proliferation.
Limitations
Slow onset of effect (weeks to months), not curative, risk of radiation-induced damage, largely
replaced by modern pharmacotherapy.
Current Role
Rare, reserved for selected refractory cases or when surgery/biologics are contraindicated.
More commonly used in Europe (radioisotope synovectomy) than in routine oncology
practice.
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Rheumatoid arthritis
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Rheumatoid arthritis
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ANEURYSMAL BONE CYSTS
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Aspect Details
Indications
- Recurrent ABC after surgery/embolization - Inoperable or surgically
inaccessible sites (spine, skull base, pelvis) - Symptomatic lesions
with pain, neurological compromise, or progressive growth
Dose - 30–36 Gy in 1.8–2 Gy/fraction (standard) - Some reports: 20–
25 Gy effective
Technique - 3D-CRT / IMRT - Target: lesion with safety margin based on CT/MRI
Outcomes - Local control: ~80–90% - Pain relief and functional/neurological
improvement - Tumor regression over months
Risks
- Rare risk of radiation-induced sarcoma (historical concern) -
Growth disturbance in young patients if growth plates irradiated -
Long-term monitoring required
ANEURYSMAL BONE CYSTS
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ANEURYSMAL BONE CYSTS
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ANEURYSMAL BONE CYSTS
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LANGERHANS CELL HISTIOCYTOSIS
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LANGERHANS CELL HISTIOCYTOSIS
Aspect Details
Indications
Symptomatic unifocal lesions (bone, orbit, CNS, spine), painful or threatening
function/structure, refractory to surgery/curettage, recurrence, or risk of
deformity.
Radiation
Sensitivity
LCH is highly radiosensitive. Even low doses can provide durable control.
Dose (Common
Range)
6–10 Gy in 1.5–2 Gy fractions for local control. In selected resistant or
recurrent cases, up to 15–20 Gy. Higher doses usually not required.
Technique
Conformal RT or modern techniques (IMRT/VMAT) for critical structures. Photons
(orthovoltage, electrons, or megavoltage depending on depth).
Response High local control (>90%) with pain relief and functional preservation.
Toxicity
Minimal due to low doses. Long-term risk of growth disturbances in children,
cataract (if orbit treated), and second malignancy risk (rare but relevant in
pediatric cases).
Special Notes
RT should be considered only when less toxic options (surgery, steroids,
chemotherapy) are inadequate or contraindicated. In children, careful justification
and dose minimization are critical.
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LANGERHANS CELL HISTIOCYTOSIS
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LANGERHANS CELL HISTIOCYTOSIS
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Gynecomastia
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Gynecomastia
Aspect Details
Indication
Painful gynecomastia, prophylaxis in men on
antiandrogen therapy (e.g., prostate cancer)
Dose
Single fraction 8–12 Gy; 10–12 Gy in 2
fractions; 20 Gy in 5 fractions
Technique Electron beam (6–9 MeV) with bolus; field over
nipple–areolar complex; lung/heart shielding
Effectiveness Prevents gynecomastia in ~70–80%; relieves pain
in ~60–80%
Toxicity Mild erythema, tenderness, nipple color change;
rare fibrosis; very low carcinogenic risk
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Gynecomastia
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Gynecomastia
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Cardiac Arrhythmia - medical resistance
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Cardiac Arrhythmia - SBRT
Aspect Details
Indication Refractory ventricular tachycardia (post-drug and failed catheter
ablation)
Target Arrhythmogenic scar/substrate (20–40 cc), defined by
electroanatomic map + MRI/PET
Dose 25 Gy in 1 fraction (most common)
Procedure
Multidisciplinary planning → 4D-CT with ECG/respiratory gating
→ image fusion → SBRT/VMAT/CK delivery with ECG monitoring
Follow-up
ECG/Holter, echo, MRI; effect appears over weeks to months
(blanking period)
Toxicity Acute: fatigue, nausea, rare pericarditis; Late: pericardial
effusion, coronary or valvular injury (under study)
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Cardiac Arrhythmia - SBRT
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Cardiac Arrhythmia - SBRT
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Choroidal hemangioma
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Choroidal hemangioma
Aspect Details
Indication
Symptomatic circumscribed or diffuse choroidal hemangioma causing
vision loss, exudative retinal detachment, or when other treatments (laser,
PDT, anti-VEGF) fail.
Techniques
External beam radiotherapy (EBRT), Plaque brachytherapy (Ru-106, I-125),
Proton beam therapy, Stereotactic radiotherapy.
Typical Dose
- EBRT: 20–25 Gy in 10 fractions (commonly used, safe for macula/optic
nerve). - Plaque brachytherapy: 30–40 Gy to tumor apex. - Proton therapy:
~20–25 Gy in 5 fractions.
Procedure
- Immobilization with retrobulbar anesthesia or mask fixation. - Imaging
(OCT, ultrasound, fundus) to define target. - Small margins applied; sparing
of lens and optic nerve prioritized. - Delivered with precise conformal
techniques.
Response
High rates of retinal reattachment and resolution of subretinal fluid;
improvement or stabilization of vision in majority of patients.
Toxicities
Generally mild; may include radiation retinopathy, optic neuropathy,
cataract (less with low doses).
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Choroidal hemangioma
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Choroidal hemangioma
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Carotid-cavernous fistula (CCF)
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Carotid-cavernous fistula (CCF)
Aspect Details
Indication
Indirect (dural) CCF, failed/contraindicated embolization, poor
surgical candidates
Mechanism Radiation induces endothelial proliferation and fibrosis →
gradual fistula closure
Dose
SRS: 18–20 Gy single fraction; Fractionated RT:
30–45 Gy in 15–25 fractions
Procedure
CT/MRI fusion → target cavernous sinus → conformal/SRS
planning → optic pathway sparing
Outcome
Closure in ~60–80% over 6–18 months; improvement in
proptosis, chemosis, diplopia
Toxicity
Usually mild; rare optic neuropathy, cranial nerve palsy,
temporal lobe necrosis
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Carotid-cavernous fistula (CCF)
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Carotid-cavernous fistula (CCF)
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Medical Refractory Epilepsy
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Aspect Details
Indication Drug-resistant mesial temporal lobe epilepsy, usually
associated with mesial temporal sclerosis
Target
Amygdala and anterior hippocampus (sometimes
parahippocampal gyrus)
Dose 20–24 Gy in a single fraction (Gamma Knife or
LINAC SRS)
Procedure - MRI-based target delineation
Medical Refractory Epilepsy
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Medical Refractory Epilepsy
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Medical Refractory Epilepsy
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PARKISONIAN TREMOR
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PARKISONIAN TREMOR
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PARKISONIAN TREMOR
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PARKISONIAN TREMOR
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TRIGEMINAL NEURALGIA
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TRIGEMINAL NEURALGIA
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TRIGEMINAL NEURALGIA
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TRIGEMINAL NEURALGIA
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CAVERNOMA
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Aspect Details
Indications
• Deep/eloquent cavernomas (brainstem, thalamus, basal
ganglia) • High surgical risk or patient refusal of surgery •
Recurrent symptomatic hemorrhage • Intractable seizures not
controlled with drugs and not suitable for surgery •
Residual/recurrent cavernoma after incomplete resection
Dose
• Single fraction (SRS): Margin dose 12–16 Gy (commonly
15–16 Gy), Max dose ~30–32 Gy
• Hypofractionated SRT: 18–24 Gy in 3–5 fractions (used near
critical structures e.g., brainstem)
Procedure
• MRI (T1, T2, GRE/SWI) + CT fusion for planning • Stereotactic
frame or frameless mask immobilization • Target = cavernoma
nidus (core + hemosiderin rim), no margin expansion • Conformal
planning with steep dose fall-off • Delivered via Gamma Knife,
LINAC, or CyberKnife • Follow-up MRI: 6–12 months, then yearly
CAVERNOMA
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CAVERNOMA
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CAVERNOMA
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INTRACRANIAL EPIDERMOID CYST
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INTRACRANIAL EPIDERMOID CYST
Scenario Preferred Treatment Radiation Role Dose / Technique
Primary (newly
diagnosed, resectable)
Maximal safe
microsurgical excision Not indicated –
Residual cyst after
surgery
Observation ± re-
surgery
Consider SRS in select
cases
SRS: 12–14 Gy single
fraction (margin dose)
Recurrent cyst (multiple
surgeries done)
Limited surgery if
feasible SRS reasonable option SRS: 11–14 Gy
Inoperable cyst (critical
location or comorbidity)
Conservative
management
SRS possible SRS: 12–13 Gy
Malignant
transformation
(epidermoid →
squamous cell
carcinoma)
Surgery + RT ± chemo
Definitive/Adjuvant
EBRT
60–66 Gy / 30–33
fractions (IMRT/VMAT)
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INTRACRANIAL EPIDERMOID CYST
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INTRACRANIAL HAMARTOMA
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INTRACRANIAL HAMARTOMA
WhatsAppVideo2025-06-27at20.25.14.mp4
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INTRACRANIAL HAMARTOMA
Step / Parameter Typical Practice
Imaging MRI (T1, T2, contrast-enhanced) fused with CT for target delineation
Target definition
Hamartoma core (avoid optic chiasm, pituitary stalk, hypothalamus margins
as much as possible)
Immobilization Frame-based (Gamma Knife) or frameless mask (LINAC/CyberKnife)
Planning system High-resolution stereotactic planning with MRI fusion
Prescription dose 14–18 Gy to lesion margin (50% isodose line)
Optic apparatus dose < 8–10 Gy (single fraction limit)
Dose conformity
Conformal planning with steep fall-off (multiple isocenters/shots in GK, non-
coplanar arcs in LINAC, robotic beams in CK)
Treatment time Typically 1–2 hours depending on system and complexity
Procedure
- Apply stereotactic frame (GK) or mask (LINAC/CK)- Acquire stereotactic
MRI/CT- Target delineation and plan optimization- Quality assurance and
dose verification- Single session delivery
Follow-up MRI at 6–12 monthsSeizure response often after 6–24 months latency
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INTRACRANIAL HAMARTOMA
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INTRACRANIAL HAMARTOMA
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GLOMUS JUGULARAE
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GLOMUS JUGULARAE
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GLOMUS JUGULARAE
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GLOMUS JUGULARAE
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CHORDOMA
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CHORDOMA CASE SELECTION
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CHORDOMA CASE SELECTION
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CHORDOMA CASE SELECTION
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ACOUSTIC NEUROMA
1. An acoustic neuroma is a noncancerous growth that develops on the
eighth cranial nerve.
2. Also known as the vestibulocochlear nerve, it connects the inner ear
with the brain and has two different parts.
3. One part is involved in transmitting sound; the other helps send balance
information from the inner ear to the brain.
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ACOUSTIC NEUROMA
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ACOUSTIC NEUROMA
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MENINGIOMAS
• Meningiomas are generally benign lesions that account for 15–20 % of
primary brain tumors, affect predominately middle- aged patients, and
occur predominately in females
• The atypical and malignant meningiomas are characterized by successive
recurrences and an aggressive behavior.
• Among all meningiomas, their incidence varies in the literature ranging
from 4.7 to 7.1 % and 1.0 to 3.7 % for atypical and malignant, respectively
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MENINGIOMA
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MENINGIOMA
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Meningioma
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ARTERIOVENOUS MALFORMATIONS
• Radiosurgery is an effective alternative treatment for selected AVM patients rather
than microsurgery , especially in those with surgically inaccessible lesions with
comorbidities which hinder surgical intervention or if microsurgery is not feasible.
• In terms of radiobiology, AVM are late responding target within late reaction of
normal tissue.
• Following bleeding , part of nidus may be hidden or compressed by clots hence it is
rational to wait till resolution of hematoma (average 2-3 months).
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AVM MX ALGORITHM-ISRS GUIDELINES
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ARTERIOVENOUS MALFORMATIONS
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ARTERIOVENOUS MALFORMATIONS
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Summary
• There is a role of Radiation in benign diseases
• Many sites are under explored
• Practice with caution
• Mostly indicated in refractory/recurrent cases
• Practice with caution in young population
• Follow guideline
• More awareness required in both physician and
population groups
• Do not forget about radiation induced malignancy
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EITHER INFLAMMATION
OR BENIGN CONDITION
WHEN THERE IS NO OPTION
CONSIDER RADIATION
LOW DOSE RADIATION
IN REFRACTORY CONDITION
EVIDENCE WITH CAUTION
YOU MAY GET SOME SOLUTION
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RADIATION BEYOND INDICATION(BENIGN DISEASES)