A 12-year-old with right groin pain and a limp

Last updated: November 27, 2025Bookmark

A 12-year-old boy was brought to the clinic with 1 1-month history of left groin pain and a limp.

Q1. What is the difference between pain that radiates into the groin and pain that originates in the groin?

Reveal Answer

Pain radiating to the groin suggests urologic, reproductive or spinal etiology

Pain originating in the groin suggests pathology in or around the hip joint

True groin pain is proximal and medial. Clarify whether the hip pain is proximal and lateral vs medial. Pain that is lateral may be due to trochanteric bursitis, neurogenic claudication, sciatica or sacroiliac joint pathology

Similarly, in the shoulder joint, pain from glenohumeral arthritis is felt medially in the axilla, while that from rotator cuff or subacromial bursitis is felt laterally over the shoulder.

Q2. What are the differentials for groin pain with refusal to bear weight in a child?

Reveal Answer

Mechanical

DifferentialsClinical features
Slipped upper femoral epiphysis (SUFE)Obese adolescent male (10 – 16 years due to rapid growth) with groin pain radiating to the knee, painful limp, and externally rotated hip. May allow range of motion. Affects the left hip more than the right.
Perthes diseaseGradual progressive limp with slow onset of pain, decreased range of motion. Peak incidence at 4 – 8 years.
Developmental dysplasia of the hipPositive Barlow and Ortolani, Galeazzi sign, positive Trendelenburg sign, delayed walking or abnormal gait if left untreated. Screening is done at birth and is unusual to be picked up at 12 years old
Stress frActurePain associated with activity or repeated loading, no history of recent truma, local tenderness and swelling

Infectious

DifferentialsDescription
Septic arthritis or osteomyelitisFever, pain and inability to move or bear weight, may have underlying joint disease e.g. Rheumatoid arthritis
Psoas abscessFever, hip flexed and internally rotated, pain on passive hip extension, associated with osteomyelitis of the spine or pelvic inflammatory disease

Inflammatory

DifferentialsDescription
Juvenile idiopathic arthritisNon-migratory arthritis affecting one or more joints for > 3 months, morning stiffness, fever
Transient synovitisMost common cause of hip pain. History of viral infection, hip pain worse on waking and improves as day progresses, self-limiting. Peak incidence at 2 – 5 years (maximum around 12 years).

Benign neoplasm

DifferentialsDescription
Osteoid osteomaContinous, deep, aching bone pain affecting the neck or back; unexplained, rigid, painful scoliosis

Malignant neoplasm

DifferentialDescription
OsteosarcomaMost common primary malignant bone tumour. Common in adolescents. Presents with deep bone pain that progresses to palpable bony mass. Affects the distal femur
Ewing sarcomaAffects children aged 5 – 15 years, bone pain, fever, fatigue, weight loss, pathologic fractures and a palpable mass

The most important differential is septic arthritis since it can cause irreversible damage to cartilage. History of fever, refusal to bear weight and laboratory values (+ Kocher criteria) can be used to confirm this diagnosis.

Q3. What questions are important to ask for in this child’s history?

Reveal Answer

History of fever (to rule out infection e.g. septic arthritis)

Recent history of viral illness (to rule out transietn synovitis)

Family history of joint disease (to rule out conditions such ad DDH and juvenile idiopathic arthritis)

Medications (a history of steroid use can predispose to perthes disease)

The pain began in his left groin and radiated to the left knee. It has been gradually increasing in intensity. It is worse with walking and relieved by rest. There is no history of trauma. He does not have pain in other joints or extremities. There is no history of recent infection, no history of fever, chills or malaise. He participates in physical education in school but is otherwise not involved in sports. He has no history of travel or camping trips and lives in an urban area. He takes no medication. There is no family history of joint problems.

On physical examination, he is afebrile and appears obese. The left lower extremity is externally rotated, abducted and flexed, and he resists internal rotation. There is no leg length discrepancy. Neurologic and vascular examination is normal.

Q4. What are the steps in the orthopaedic examination of a painful hip?

Reveal Answer

Gait

Look (inspection – attitude and leg length)

Feel (palpation of the ASIS, trochanteric bursa and muscle insertions)

Move (active and passive range of motion)

Neurologic (motor and sensory)

Vascular (pulses)

Special tests

Q5. List three special tests used to examine the hip

Reveal Answer
TestDescription
Thomas testTest for flexion contracture. With the patient lying suine one knee is brougth to the chest. If the opposite leg is unable to remain extended there is flexion contracture of the hip
Trendelenburg testPatient stands in position and lifts one leg. If the pelvis falls on the side of the raised leg there is abductor weakness on the side of the standing leg (contralateral)
FABERFlexion, abduction and external rotation of the hip with the patient lying supine. Pain during this movement suggests sacroiliac joint pathology.

Q6. What is the most likely diagnosis?

Reveal Answer

Slipped upper femoral epiphysis (SUFE) affecting the right lower extremity

Age 12 years (period of rapid growth)

Non-traumatic groin pain radiating to the knee

External rotation and abduction of the hip with flexion (Drehmann’s sign)

Resistance to internal rotation

SUFE is displacement of the metaphysis of the femoral neck from teh epiphysis through the growth plate (physis). Commonly due to overloading of teh physis (oesity) or weakened growth plate (endocrine disorder). The neck displaces anteriorly and superiorly relative to teh femoral epiphysis

External rotation of the leg is the most common resting position in SUFE because of the mechanical direction of slippage. Obligate external rotation can be observed when the hip is flexed, i.e. the leg involuntarily externally rotates

Q7. External rotation of the leg is the most common resting position in SUFE. What should be considered if the limb is held in slight hip flexion and internally rotated instead?

Reveal Answer

Psoas abscess

Hip dislocation Psoas abscess is associated with fever and other signs of infection. The source of the abscess should be investigated e.g. osteomyelitis of the spine, pelvic inflammAtory disease An internally rotated and flexed hip following trauma is hip dislocation until proven otherwise. This is a surgical emergency.

Q8. In the setting of knee pain, why should the hip be examined?

Reveal Answer

Hip pathology (SUFE and perthes disease) can present with referred pain to the knee

In children, a complaint of knee pain should lead to clinical examination of the hip and a radiograph of the hip

Q9. What are the risk factors for developing SUFE?

Reveal Answer

Age 10 – 16 years

Male gender

Obesity (one of the strongest risk factor due to increased load across the physis increasing the likelihood of slippage)

50% of patients with SUFE are ≥ 90th percentile for weight.

Q10. What condition may be associated with SUFE?

Reveal Answer

Hypothyroidism

Renal osteodystrophy

Excessive growth hormone

Hypopituitarism

Hyper- or hypoparathyroidsm

These conditions physiologically weaken the physis, leading to slippage

With these conditions, SUFE can present early (< 10 years) or later (> 16 years) in life

Suspect endocrine disease in young thin patients (delayed growth or puberty)

Q11. What investigations are useful in this case?

Reveal Answer

Pelvic X-ray (AP and frog-leg lateral view) +/- knee radiographs

Complete blood count and CRP: to rule out infection (septi carthritis)

Blood culture and joint aspiration: if there is suspiscion of infection

Knee radiographs (AP, lateral and sunrise view) can be added if knee pathology is suspected

MRI can be used to rule out non-displaced stress fractures, early necrosis in Perthes disease, soft tissue abnormalities of the ligaments, tendons and labrum, and bone tumours.

CT is used sparingly due to the risk of unnecessary exposure to radiation

A bone scan can be used for osteomyelitis or a tumour

Q12. What are the classic radiographic findings in SUFE vs DDH vs Perthes disease?

Reveal Answer
ConditionRadiographic findings
Slipped upper femoral epiphysis (SUFE)Klein’s line does not intersect the femoral head, growth plate widening or lucency (epiphysiolysis), blurring of the femoral metaphysis (metaphyseal blanch sign of steel)
Developmental dysplasia of the hip (DDH)Difficult to assess on X-ray for infants but – disrupted shenton’s line, femoral head ossification superior to Hilgenreiner’s line, femoral head ossification lateral to perkin’s line, delayed ossification of teh femoral head, absent acetabular teardrop
Perthes diseaseSubchondral collapse, flattening and fragmentation of the femoral head
Kline’s line in slipped upper femoral epiphysis

Q13. What is the treatment of SUFE vs DDH vs Perthes disease?

Reveal Answer

ConditionTreatment
Slipped upper femoral epiphysis (SUFE)Percutaneous in situ screw fixation through the femoral neck, contralateral in sity prophylactic pinning (bilateral in situ fixation)
Developmental dysplasia of the hip (DDH)Abduction bracing with a Pavlik harnss for < 6 months, open/closed recution and spica cast for 6 – 18 mothns, open reduction and pelvic osteotomy for > 18 months
Perthes diseaseMost require supportive treatment, advanced disease can be contained with abduction bracing or pelvic/femoral osteotomies

Q14. What are the complications of SUFE?

Reveal Answer

Osteonecrosis of the femoral head

Contralateral SCFE/SUFE

Chondrolysis

Slip progression

Infection

Chronic pain

Degenerative arthritis

Pin associated proximal femur fracture

Labral tearing and degeneration

Reference Intervals
Biochemistry
ACTHP: <80 ng/L
ALTP: 5–35 U/L
AlbuminP: 35–50 g/L
AldosteroneP: 100–500 pmol/L
Alk. phosphataseP: 30–130 U/L
α-AmylaseP: 0–180 IU/dL
α-FetoproteinS: <10 kU/L
Angiotensin IIP: 5–35 pmol/L
ADHP: 0.9–4.6 pmol/L
ASTP: 5–35 U/L
BicarbonateP: 24–30 mmol/L
BilirubinP: 3–17 μmol/L
BNPP: <50 ng/L
CRPP: <10 mg/L
CalcitoninP: <0.1 mcg/L
Calcium (ionized)P: 1.0–1.25 mmol/L
Calcium (total)P: 2.12–2.60 mmol/L
ChlorideP: 95–105 mmol/L
CholesterolP: <5.0 mmol/L
VLDLP: 0.128–0.645 mmol/L
LDLP: <2.0 mmol/L
HDLP: 0.9–1.93 mmol/L
Cortisol AMP: 450–700 nmol/L
Cortisol MidnightP: 80–280 nmol/L
CK ♂P: 25–195 U/L
CK ♀P: 25–170 U/L
CreatinineP: 70–100 μmol/L
FerritinP: 12–200 mcg/L
FolateS: 2.1 mcg/L
FSHP: 2–8 U/L ♂; >25 menopause
GGT ♂P: 11–51 U/L
GGT ♀P: 7–33 U/L
Glucose (fasting)P: 3.5–5.5 mmol/L
Growth hormoneP: <20 mu/L
HbA1C (DCCT)B: 4–6%
HbA1C (IFCC)B: 20–42 mmol/mol
Iron ♂S: 14–31 μmol/L
Iron ♀S: 11–30 μmol/L
Lactate (venous)P: 0.6–2.4 mmol/L
Lactate (arterial)P: 0.6–1.8 mmol/L
LDHP: 70–250 U/L
LHP: 3–16 U/L
MagnesiumP: 0.75–1.05 mmol/L
OsmolalityP: 278–305 mosmol/kg
PTHP: 0.8–8.5 pmol/L
PotassiumP: 3.5–5.3 mmol/L
Prolactin ♂P: <450 U/L
Prolactin ♀P: <600 U/L
PSAP: 0–4 mcg/mL
Protein (total)P: 60–80 g/L
Red cell folateB: 0.36–1.44 μmol/L
Renin (erect)P: 2.8–4.5 pmol/mL/h
Renin (recumbent)P: 1.1–2.7 pmol/mL/h
SodiumP: 135–145 mmol/L
TBGP: 7–17 mg/L
TSHP: 0.5–4.2 mU/L
T4P: 70–140 nmol/L
Free T4P: 9–22 pmol/L
TIBCS: 54–75 μmol/L
TriglyceridesP: 0.50–2.3 mmol/L
T3P: 1.2–3.0 nmol/L
Troponin TP: <0.1 mcg/L
Urate ♂P: 210–480 μmol/L
Urate ♀P: 150–390 μmol/L
UreaP: 2.5–6.7 mmol/L
Vitamin B12S: 0.13–0.68 nmol/L
Vitamin DS: 50 nmol/L
Arterial Blood Gases
pH7.35–7.45
PaCO₂4.7–6.0 kPa
PaO₂>10.6 kPa
Base excess±2 mmol/L
Urine
Cortisol (free)<280 nmol/24h
Hydroxyindole acetic acid16–73 μmol/24h
Hydroxymethylmandelic acid16–48 μmol/24h
Metanephrines0.03–0.69 μmol/mmol cr.
Osmolality350–1000 mosmol/kg
17-Oxogenic steroids ♂28–30 μmol/24h
17-Oxogenic steroids ♀21–66 μmol/24h
17-Oxosteroids ♂17–76 μmol/24h
17-Oxosteroids ♀14–59 μmol/24h
Phosphate (inorganic)15–50 mmol/24h
Potassium14–120 mmol/24h
Protein<150 mg/24h
Protein/creatinine ratio<3 mg/mmol
Sodium100–250 mmol/24h
Haematology
WCC4.0–11.0 ×10⁹/L
RBC ♂4.5–6.5 ×10¹²/L
RBC ♀3.9–5.6 ×10¹²/L
Hb ♂130–180 g/L
Hb ♀115–160 g/L
PCV ♂0.4–0.54 L/L
PCV ♀0.37–0.47 L/L
MCV76–96 fL
MCH27–32 pg
MCHC300–360 g/L
RDW11.6–14.6%
Neutrophils2.0–7.5 ×10⁹/L (40–75%)
Lymphocytes1.0–4.5 ×10⁹/L (20–45%)
Eosinophils0.04–0.44 ×10⁹/L (1–6%)
Basophils0–0.10 ×10⁹/L (0–1%)
Monocytes0.2–0.8 ×10⁹/L (2–10%)
Platelets150–400 ×10⁹/L
Reticulocytes0.8–2.0% / 25–100 ×10⁹/L
Prothrombin time10–14 s
APTT35–45 s
Paediatric
Pulse Rate (bpm)
Neonate140–160
Infant <1yr120–140
1–5 years110–130
5–12 years80–120
>12 years70–100
Respiratory Rate (tachypnoea)
0–2 months≥60/min
2–12 months≥50/min
1–5 years≥40/min
>5 years≥30/min
Blood Pressure (mmHg)
Term65/45
1 year75/50
4 years85/60
8 years95/65
10 years100/70
Weight Formulas
3–12 months(a + 9)/2 kg
1–6 years2a + 8 kg
>6 years(7a − 5)/2 kg
Haemoglobin (g/dL)
Term newborn13–20
1 month11–18
2 months10–15
1–2 years10–13
>2 years11–14
MUAC (6 months–5 years)
Obese>17.5 cm
Normal13.5–17.4 cm
At risk12.5–13.4 cm
Moderate malnutrition11.5–12.4 cm
Severe malnutrition<11.5 cm
Developmental Milestones
Social smile1.5 months
Head control4 months
Sits unsupported7 months
Crawls10 months
Stands unsupported10–12 months
Walks12–13 months
Talks18 months
CSF WBC (/mm³)
Term newborn0–25
>2 weeks0–5
Calculator

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