Rheumatology Flashcards

(80 cards)

1
Q

Hi there 🫡 Ψ³Ω…Ω‘ΩΩŠ Ψ§Ω„Ω„Ω‡

A

Ψ¨Ψ³Ω… Ψ§Ω„Ω„Ω‡ Ψ§Ω„Ψ±Ψ­Ω…Ω† Ψ§Ω„Ψ±Ψ­ΩŠΩ… πŸ’‘

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2
Q

What is Juvenile Idiopathic Arthritis (JIA) ⁉️

A

🧠 Chronic arthritis in children <16 years old , lasting β‰₯6 weeks
⚠️ Diagnosis of exclusion
## footnote
πŸ” Must rule out: infection, malignancy, trauma, systemic diseases, post-infectious causes

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3
Q

What are the main subtypes of JIA and their criteria ⁉️

A

πŸ”Έ Oligoarticular JIA : ≀4 joints
πŸ”Έ Polyarticular JIA : β‰₯5 joints
πŸ”Έ Systemic-onset JIA :
 ‒ High spiking fever β‰₯2 weeks
 ‒ Salmon-pink rash , arthritis
 ‒ Hepatosplenomegaly, serositis

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4
Q

What are the typical joint symptoms of JIA ⁉️

A

🦴 Painful, tender, warm, swollen joints
⏰ Worse in the morning
🚢 Limping often seen
## footnote
⚠️ Symptoms persist β‰₯6 weeks

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5
Q

What systemic symptoms are seen in systemic-onset JIA ⁉️

A

πŸ”₯ Daily fever spikes
πŸ”΄ Salmon-colored, non-pruritic rash
🧬 Serositis: pleuritis, pericarditis, ascites
πŸ«€ Hepatosplenomegaly

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6
Q

How is JIA diagnosed ⁉️

A

πŸ§ͺ Clinical diagnosis β€” no definitive test
⚠️ Must rule out:
 ‒ Infection, SLE, leukemia, reactive arthritis
 ‒ HSP, osteomyelitis, sarcoidosis
πŸ§ͺ RF, ESR, CRP may help classify but are not diagnostic

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7
Q

What is the importance of uveitis screening in JIA ⁉️

A

πŸ‘ Uveitis = inflammation of uveal tract
⚠️ Risk highest in oligo/polyarticular JIA <7 years with positive ANA

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8
Q

What is the recommended frequency of eye screening for uveitis in JIA ⁉️

A

πŸ“… Systemic JIA: Every 12 months
πŸ“… Oligo/Poly JIA >7 yrs OR ANA-negative: Every 6 months
πŸ“… Oligo/Poly JIA <7 yrs & ANA-positive: Every 3–4 months

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9
Q

What is the treatment approach for mild JIA ⁉️

A

πŸ’Š NSAIDs
πŸ’‰ Intra-articular corticosteroid injections

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10
Q

What is the treatment for systemic-onset JIA ⁉️

A

πŸ’Š Oral/IV corticosteroids
🧬 Biologics (e.g., anakinra , IL-1 inhibitors)
🧠 Add methotrexate as a disease-modifying agent

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11
Q

What are the key clinical features of juvenile psoriatic arthritis ⁉️

A

🦴 Arthritis in small and large joints
🌿 Psoriatic skin rash (if present)
βœ… If rash is absent ➑️ Look for:
 ‒ Family history of psoriasis
 ‒ Nail pitting
 ‒ Dactylitis (β€œsausage digit”)

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12
Q

What are the recommended screening and labs in juvenile psoriatic arthritis ⁉️

A

πŸ‘οΈ Uveitis risk ➑️ Screen with slit-lamp exam every 6 months
πŸ§ͺ Lab tests:
 ‒ ANA
 ‒ HLA-B27

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13
Q

What is Enthesitis-Related Arthritis (ERA) and who is typically affected ⁉️

A

🧠 A subtype of JIA seen in older children >8 years
🦴 Associated with pain, stiffness, and limited mobility of the lower back
πŸ“ Commonly involves sacroiliac joints and lower extremity arthritis

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14
Q

What lab marker is commonly positive in Enthesitis-Related Arthritis ⁉️

A

πŸ§ͺ HLA-B27 positive
🧠 Strong genetic association, similar to adult spondyloarthropathies

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15
Q

A 15-year-old develops monoarthritis a week after Streptococcus group G pharyngitis. What is the most probable diagnosis ⁉️

A

βœ… Post-streptococcal reactive arthritis (PSRA)
## footnote
🧠 Clues:
β€’ Group G strep (not group A β†’ excludes ARF)
β€’ No migratory pattern , no major Jones criteria
β€’ Incomplete response to NSAIDs
β€’ Monoarthritis in a teenager
➑️ PSRA is a non-rheumatic post-infectious arthritis

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16
Q

What is the recommended treatment for post-streptococcal reactive arthritis ⁉️

A

πŸ’Š NSAIDs (often insufficient alone)
πŸ’‰ Short course of steroids may be needed
## footnote
🚫 No clear indication for long-term prophylaxis like ARF

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17
Q

What are the clinical features of septic arthritis in children ⁉️

A

🚨 Ill-appearing child
πŸ”₯ High-grade fever >38.5Β°C
πŸ“ˆ CRP : elevated
🩸 WBC : >12,000 cells/mL
❌ Unable to bear weight
❌ Refuses to move joint
🩻 Pain with extreme rotation
## footnote
πŸ’Š Rx: Antibiotics + surgical drainage

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18
Q

What are the clinical features of transient synovitis in children ⁉️

A

😊 Well-appearing child
🌑️ Mild or no fever
πŸ“‰ CRP: normal or slightly raised
🩸 WBC: normal or slightly elevated
βœ… Able to bear weight
🦴 Restricted abduction
🦠 Often follows recent URTI
πŸ’Š Rx: Analgesics + bed rest (self-limiting)

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19
Q

What is the most distinguishing clinical difference between septic arthritis and transient synovitis ⁉️

A

🧠 Septic arthritis : child is toxic, febrile, cannot bear weight
🧠 Transient synovitis : child is well, afebrile or mildly febrile, can bear weight

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20
Q

What are the key clinical features of Systemic Lupus Erythematosus (SLE) ⁉️

A

πŸ”» Photosensitivity
πŸ”» Painless oral ulcers
πŸ”» Malar rash (butterfly-shaped)
πŸ”» Non-erosive arthritis
πŸ”» Serositis (pleuritis or pericarditis)
πŸ”» Renal disorder (persistent proteinuria)
πŸ”» Neurologic disorder (e.g., seizures)
πŸ”» Hematologic disorder (anemia, leukopenia, lymphopenia)

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21
Q

Which autoantibodies are important in the diagnosis of SLE ⁉️

A

πŸ§ͺ Anti-dsDNA β†’ diagnostic & used to monitor disease activity
πŸ§ͺ Anti-Smith (Sm) β†’ highly specific
πŸ§ͺ ANA β†’ very sensitive (positive in ~99% of SLE cases)

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22
Q

What complement levels are associated with SLE disease activity ⁉️

A

πŸ“‰ C3 and C4 are low or undetectable during active disease
## footnote
🧠 Useful for monitoring disease flares

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23
Q

How is SLE managed in children ⁉️

A

πŸ’Š Hydroxychloroquine (first-line for skin/joint symptoms)
πŸ’Š Corticosteroids for flares
πŸ’Š Cyclophosphamide or other immunosuppressants for severe organ involvement
πŸ’Š NSAIDs for arthritis
βž• Supportive:
 ‒ Monitor BP & renal function
 ‒ Calcium + Vitamin D
 ‒ No live vaccines if immunosuppressed
 ‒ School accommodations, diet, and vitamin support

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24
Q

Which antibody is most specific for diagnosing SLE ⁉️
A. ANA
B. Anti-dsDNA
C. Rheumatoid factor
D. Anti-Smith antibody

A

πŸ‘
D. Anti-Smith antibody
## footnote
Anti-Smith (Sm) antibody is highly specific for SLE, although not always present.

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25
**What causes Neonatal Lupus Erythematosus (NLE)** ⁉️
πŸ‘©β€πŸΌ Caused by **transplacental passage** of maternal autoantibodies: πŸ§ͺ **Anti-SSA (Ro)** or **Anti-SSB (La)** 🧠 Can occur even if the mother is asymptomatic
26
**What are the clinical manifestations of neonatal lupus** ⁉️
πŸ”» **Rash** (transient) πŸ’“ **Congenital heart block** (seen in ~30%) 🩺 **Fetal bradycardia** may be the first sign 🧠 Heart block is often **irreversible**
27
**What is the long-term prognosis in neonatal lupus** ⁉️
βœ… Most **non-cardiac symptoms resolve by 6 months** 🚨 **Heart block does not resolve** ➑️ **30–50%** of affected infants require a **pacemaker**
28
**What is the management for fetal heart block due to NLE** ⁉️
πŸ’Š **Dexamethasone** may be given prenatally βš™οΈ **Pacemaker** may be needed postnatally for symptomatic bradycardia
29
**What is the most likely ECG finding in a newborn with congenital heart block due to neonatal lupus** ⁉️
πŸ“‰ **Bradycardia** πŸ“Š **Complete AV block (3rd-degree)** ➑️ **P waves and QRS complexes dissociated** 🧠 Seen in **Lead II** with regular atrial and ventricular rates that are **independent**
30
**What maternal condition is most commonly associated with congenital heart block in neonates** ⁉️
πŸ‘©β€πŸΌ **Positive anti-Ro (SSA) or anti-La (SSB)** antibodies 🧬 Often seen in mothers with **SLE** or **SjΓΆgren’s syndrome** 🩺 May present with **rash** and/or **anti-phospholipid antibodies**
31
**A newborn has bradycardia and ECG shows complete AV block. Which maternal history explains this** ⁉️ A. Alcohol use during pregnancy B. Anti-phospholipid antibodies + rash C. CMV infection in 1st trimester D. Treated maternal hypothyroidism
πŸ‘ **B. Anti-phospholipid antibodies + rash** ## footnote Anti-Ro/SSA antibodies in mothers with SLE or SjΓΆgren’s cause neonatal lupus β†’ congenital heart block.
32
**What are the hallmark clinical features of ankylosing spondylitis (AS)** ⁉️
🦴 **Inflammatory low back pain** ⏰ Worse in the **morning** , improves with **exercise** πŸ“ˆ **Elevated ESR & CRP** 🧬 Associated with **HLA-B27**
33
**What radiologic findings are characteristic of ankylosing spondylitis** ⁉️
πŸ“Έ **Sacroiliitis with sclerosis** πŸͺ΅ **β€œBamboo spine”** due to **bridging syndesmophytes** 🧠 Axial skeleton involvement is progressive
34
**What is the genetic marker strongly associated with ankylosing spondylitis** ⁉️
🧬 **HLA-B27** positivity βœ… Found in most patients with AS and related spondyloarthropathies
35
**What are the classic clinical features of SjΓΆgren syndrome in children vs adults** ⁉️
πŸ‘§πŸΌ **Children** : recurrent **parotitis** πŸ‘©πŸΌ **Adults** :  ‒ **Keratoconjunctivitis sicca** (dry eyes)  ‒ **Xerostomia** (dry mouth) 🧠 Can also cause **skin rash, arthritis**, and fatigue
36
**What autoantibodies are associated with SjΓΆgren syndrome** ⁉️
πŸ§ͺ **Anti-Ro (SSA)** πŸ§ͺ **Anti-La (SSB)** 🧠 Also seen in **neonatal lupus**
37
**What are the treatment options for SjΓΆgren syndrome** ⁉️
πŸ’§ **Artificial tears** for dry eyes πŸ’Š **Pilocarpine tablets** for dry mouth πŸ’Š **Antimalarials (e.g., hydroxychloroquine)** for rash and arthritis
38
**What is a major long-term complication of SjΓΆgren syndrome** ⁉️
🚨 **Increased risk of lymphoma** 🧠 Especially **non-Hodgkin’s B-cell lymphoma**
39
**What is the classic triad of reactive arthritis (Reiter’s syndrome)** ⁉️
🧠 **Mnemonic** : β€œCan’t see, can’t pee, can’t climb a tree” πŸ‘οΈ **Conjunctivitis** 🚻 **Urethritis** (non-infectious) 🦴 **Arthritis** (usually asymmetric, lower limb)
40
**What infections commonly precede reactive arthritis** ⁉️
⚠️ **Gastrointestinal pathogens** :  ‒ Shigella, Salmonella, Yersinia, Campylobacter ⚠️ **Genitourinary pathogens** :  ‒ Chlamydia trachomatis
41
**What is the typical time frame between infection and onset of reactive arthritis** ⁉️
⏰ **2–4 weeks** after GI or GU infection 🧠 Arthritis appears after infection has resolved
42
**What lab findings are common in reactive arthritis** ⁉️
πŸ“ˆ **Elevated ESR and CRP** 🧬 **HLA-B27 positive** in 65–96% of cases
43
**What is the treatment for reactive arthritis** ⁉️
πŸ’Š **Supportive care** :  ‒ NSAIDs  ‒ Physical therapy ❌ Antibiotics are **not** effective once arthritis develops 🧠 Chronic cases may require **DMARDs**
44
**What are the key clinical features of Juvenile Dermatomyositis (JDM)** ⁉️
🦡 **Proximal muscle weakness** (pelvic/shoulder girdle) 🌞 **Photosensitive skin rash** 🟣 **Heliotrope rash** (upper eyelids) πŸŸͺ **Gottron papules** (over knuckles) 🧊 **Calcinosis cutis** ⚠️ **GI involvement** : abdominal pain, gastritis
45
**What laboratory findings support the diagnosis of JDM** ⁉️
πŸ§ͺ **Elevated creatine kinase (CK)** πŸ“ˆ Indicates muscle inflammation and damage
46
**What is the first-line treatment for Juvenile Dermatomyositis** ⁉️
πŸ’Š **Prednisone** (corticosteroids) πŸ’Š **Hydroxychloroquine** for skin rash 🌀️ **Sun avoidance** is crucial to prevent rash flares
47
**What are Gottron papules and the heliotrope rash** ⁉️
πŸŸͺ **Gottron papules** : scaly, violet plaques over extensor surfaces of fingers 🟣 **Heliotrope rash** : violet discoloration and swelling of the eyelids
48
**What are the clinical features of systemic scleroderma in children** ⁉️
🧴 **Pruritic skin tightening** ❄️ **Raynaud’s phenomenon** πŸ₯£ **Dysphagia** (difficulty swallowing) πŸ’¨ **Shortness of breath** 🦴 **Joint pain, stiffness, limited ROM** πŸ’ͺ **Muscle weakness**
49
**What autoantibody is associated with systemic scleroderma** ⁉️
πŸ§ͺ **Anti-Scl-70** (anti-topoisomerase I) 🧠 Suggests diffuse cutaneous systemic sclerosis
50
**What is the hallmark skin lesion in localized scleroderma (morphea)** ⁉️
βš”οΈ **Linear streak on the face = β€œEn Coup de Sabre”** 🧠 Resembles a sword strike
51
**What are the systemic associations of localized scleroderma** ⁉️
🧠 **Seizures** πŸ‘οΈ **Uveitis** (eye inflammation) ⚠️ Especially if the lesion is on the face or scalp
52
**What is the treatment and prognosis of localized scleroderma** ⁉️
🧴 Mainly **supportive care** πŸƒ **Physical therapy** if joints are involved ⏳ Often **resolves spontaneously** in **3–4 years**
53
**What is the diagnostic criteria for BehΓ§et’s disease** ⁉️
πŸ”Ή **Recurrent oral ulcers β‰₯3 times in 1 year** βž• Plus **β‰₯2 of the following** : β€’ Recurrent **genital ulcers** β€’ **Eye inflammation** (e.g., anterior uveitis, hypopyon) β€’ **Characteristic skin lesions** β€’ **Positive pathergy test** (skin hyperreactivity)
54
**What are the common clinical findings in BehΓ§et’s disease** ⁉️
πŸ‘„ **Oral ulcers** 🩸 **Genital ulcers** πŸ‘οΈ **Anterior uveitis** , sometimes with **hypopyon** 🩻 Skin lesions + pathergy reaction (papule after needle prick)
55
**What is the treatment for BehΓ§et’s disease** ⁉️
πŸ’Š **Azathioprine** (Imuran) πŸ’‰ **Infliximab** in severe/refractory cases ## footnote 🧠 Aim: control inflammation and prevent vision loss or ulcers
56
**What is Henoch-SchΓΆnlein Purpura (HSP), and what type of condition is it** ⁉️
🧠 **HSP = IgA-mediated small vessel vasculitis** 🧬 Common in children 🟣 Presents with **palpable purpura** (esp. lower limbs)
57
**What are the classic features of HSP** ⁉️
πŸ”» **Purpura** (non-thrombocytopenic) 🦴 **Arthritis** or arthralgia 🩸 **GI involvement** :  ‒ Abdominal pain  ‒ GI bleeding  ‒ ⚠️ **Ileo-ileal intussusception** πŸ§ͺ **Renal** : hematuria, proteinuria (nephritis) πŸ’§ Subcutaneous & **scrotal edema**
58
**How is HSP diagnosed** ⁉️
βœ… **Clinical diagnosis** πŸ“ˆ **Platelet count** : normal or elevated 🩺 **Urinalysis** : screen for hematuria or proteinuria 🩸 **ESR** : may be elevated ⚠️ **Monitor BP & urinalysis for at least 6 months**
59
**What are the treatment options for HSP** ⁉️
πŸ’§ **Supportive** : hydration, NSAIDs for joint pain πŸ’Š **Corticosteroids** if:  ‒ Severe abdominal pain  ‒ Nephrotic-range proteinuria  ‒ Severe scrotal edema  ‒ Neurologic involvement 🧬 Immunosuppressives for **complicated renal disease**
60
**What is the prognosis and follow-up recommendation in HSP** ⁉️
βœ… Most cases resolve spontaneously 🩺 **Urine & BP monitoring** for **β‰₯6 months** ⚠️ Watch for development of **glomerulonephritis**
61
**What are the diagnostic criteria for classic Kawasaki disease** ⁉️
πŸ”₯ **Fever >5 days** βž• **β‰₯4 of the following 5 features** : 1️⃣ **Peripheral extremity changes** (erythema, edema, desquamation) 2️⃣ **Polymorphous rash** 3️⃣ **Oropharyngeal changes** (red tongue, cracked lips) 4️⃣ **Nonexudative bilateral conjunctivitis** 5️⃣ **Cervical lymphadenopathy** (often unilateral)
62
**What are common clinical and associated symptoms of Kawasaki disease** ⁉️
🧠 Core signs: β€’ Fever β€’ Rash β€’ **Strawberry tongue** β€’ **Nonexudative conjunctivitis** β€’ **Desquamation** (fingertips) βž• Associated: β€’ Abdominal pain, vomiting β€’ Hydrops of gallbladder β€’ Joint pain, irritability
63
**What lab findings support the diagnosis of Kawasaki disease** ⁉️
πŸ“ˆ **CRP β‰₯ 3.0 mg/dL** or **ESR β‰₯ 40 mm/h** πŸ“Š WBC β‰₯ 15,000/ΞΌL πŸ“‰ **Low albumin ≀ 3.0 g/dL** 🩸 **Anemia, pyuria, ↑ ALT** πŸ”Ό **Platelets β‰₯ 450,000/ΞΌL** after day 7
64
**What is the echocardiogram schedule for Kawasaki disease** ⁉️
πŸ«€ **Echocardiogram at** : 1. Diagnosis 2. 2nd week 3. 1 month after labs normalize 4. At 1 year if no coronary artery involvement πŸ‘¨β€βš•οΈ Refer to cardiologist if **any echo abnormality**
65
**What is the mainstay treatment of Kawasaki disease** ⁉️
πŸ’‰ **IVIG** 2 g/kg over 12–14 hours πŸ’Š **High-dose Aspirin** : 80–100 mg/kg/day until fever resolves ➑️ Then **low-dose aspirin** (3–5 mg/kg/day) for 6–8 weeks if no coronary involvement πŸ›‘οΈ **IVIG** : reduces risk of **coronary aneurysms** ⚠️ Monitor for anaphylaxis or aseptic meningitis
66
**What is the goal of aspirin therapy in Kawasaki disease** ⁉️
βœ… Relieve inflammation βœ… Antiplatelet effect βž• Synergistic benefit with IVIG in preventing coronary aneurysms
67
**What are the key features of growing pains in children** ⁉️
🧠 **Diagnosis of exclusion** πŸ‘§ Typically in **preschool or school-age** 🦡 **Bilateral leg/extremity pain** πŸŒ™ Pain occurs in the **evening or night** , may **wake child from sleep** β˜€οΈ **Resolves by morning** πŸƒ **No activity limitation during the day** πŸ”„ Often after **days of high physical activity**
68
**What should the physical exam and labs look like in growing pains** ⁉️
βœ… **Normal physical exam** πŸ§ͺ If concern arises (fever, limp, joint swelling):  ‒ X-ray  ‒ CBC with differential  ‒ **ESR** and **CRP** ⚠️ Helps rule out infection, malignancy, or arthritis
69
**How are growing pains managed in children** ⁉️
πŸ’¬ **Reassurance** ❄️ Ice or **heat therapy** 🀲 Massage πŸ’Š **NSAIDs** for pain relief 🧠 No need for long-term treatment
70
**What is Familial Mediterranean Fever (FMF), and how is it inherited** ⁉️
🧬 **Autosomal recessive autoinflammatory disorder** 🧠 Characterized by **recurrent episodes of fever and serositis** πŸ§‘β€πŸ‘©β€πŸ‘§ Often seen in individuals with a **positive family history**
71
**What are the key clinical features of FMF** ⁉️
πŸ”₯ **Periodic fever attacks** πŸ’’ **Severe abdominal pain** 🫁 **Pleuritis or pericarditis** 🩺 **Scrotal swelling** 🦡 **Arthritis/arthralgia/myalgia** 🩸 **Erysipelas-like rash** around the ankle
72
**What serious complication is associated with untreated FMF** ⁉️
🚨 **AA amyloidosis** ➑️ **proteinuria** , ➑️ **renal failure** πŸ§ͺ Proteinuria may be the first clue
73
**How is FMF diagnosed and monitored** ⁉️
🧠 **Clinical diagnosis** (supported by genetic testing) πŸ“ˆ During attacks: **↑ ESR, CRP, WBCs** πŸ§ͺ Monitor **urinalysis** for protein πŸ“… **Follow-up** : every 3–6 months
74
**What is the treatment of choice for FMF** ⁉️
πŸ’Š **Colchicine** βœ… Prevents attacks and reduces risk of **amyloidosis** ⚠️ Monitor for **colchicine toxicity**
75
**What is PFAPA syndrome, and at what age does it typically present** ⁉️
🧠 **Benign periodic fever syndrome** πŸ§’ Occurs between **6 months to 7 years** (mean age ~3 years) πŸ”₯ **Fever episodes** last **5–7 days** , recur every **<4 weeks** βœ… Child appears **healthy between episodes**
76
**What are the hallmark features of PFAPA** ⁉️
πŸ” **Recurrent periodic fever** πŸ‘„ **Aphthous stomatitis** (mouth ulcers) πŸ‘ƒ **Pharyngitis** (sore throat) 🦠 **Cervical lymphadenitis** (swollen neck nodes) πŸ§ͺ **No signs of active infection**
77
**How is PFAPA diagnosed** ⁉️
🧠 **Clinical diagnosis** πŸ§ͺ Labs may show mild elevation in CRP/ESR during flares πŸ§’ **No specific test** , and cultures are negative
78
**What are the treatment options for PFAPA** ⁉️
πŸ’Š **Single dose of steroids** (e.g. prednisolone) πŸ’Š **NSAIDs** for fever control βš”οΈ **Tonsillectomy** may eliminate episodes in some cases
79
**What is the prognosis of PFAPA** ⁉️
βœ… **Self-limiting** – typically resolves by **teenage years** 🧠 No long-term complications
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