Common Orthopaedic Deformities PDF
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Ain Shams University
Nabil Ghaly
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This document provides an overview of common orthopaedic deformities, including causes, symptoms, and treatments for conditions like genu varum (bow legs), genu valgum (knock knees), hip deformities, and elbow deformities. It also covers bone softening diseases such as osteogenesis imperfecta and rickets. The material is presented in a lecture format.
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# Common Orthopaedic Deformities ## Prof. Dr. Nabil Ghaly Professor of Orthopaedic Surgery Ain Shams University - A deformity is the deviation from the normal appearance of a part of the body. - Common orthopaedic deformities are either congenital or acquired. - Most deformities may require surgic...
# Common Orthopaedic Deformities ## Prof. Dr. Nabil Ghaly Professor of Orthopaedic Surgery Ain Shams University - A deformity is the deviation from the normal appearance of a part of the body. - Common orthopaedic deformities are either congenital or acquired. - Most deformities may require surgical intervention. ## The Knee - **Genu Varum (Bow leg):** - **In infants:** - the most common cause is developmental and physiologic. - The deformity gradually corrects with growth over months, almost correcting completely by the age of 4 years. - No treatment is necessary. - **In children (aged 1.5-2 years):** - Rickets is the commonest cause. - It is associated with its systemic signs, symptoms and laboratory findings. - Treatment is directed to correcting the cause; usually vitamin D deficiency. - In some advanced cases osteoclasis or osteotomy is required. - **In adults:** - Osteoarthritis - Mal-united fracture - Ligamentous injury - Paget's disease are the main causes. - Treatment is also directed at surgical correction of the deformity. - **Genu Valgum (knock knees):** - **Valgus knee up to the age of 4 years:** - Usually developmental or physiological. - Almost always corrects itself by 6-8 years. - If the condition is still progressive at that age, a supracondylar osteotomy of the femur is required. ## The Hip - The normal neck-shaft angle of the proximal femur is 160° at birth, decreasing to 125° at adulthood. - An angle less than 110° is called **coxa vara**. - An angle more than 130° is called **coxa valga**. - They both lead to gait disability and secondary spinal pain and deformity. - Treatment is by corrective subtrochanteric osteotomy. ## The Elbow - The normal carrying angle is 10-15 degrees of valgus, which allows a clearing distance for objects to be carried by hand alongside the trunk while walking. - An angle above that will cause **cubitus valgus**, and below it **cubitus varus**. - These deformities are corrected surgically through a wedge osteotomy at the lower humerus. ## Bone Softening Diseases - The bone is a type of connective tissue formed of cells and matrix. - **Bone cells are mainly 2 types:** - Bone forming cells (osteoblasts). - Bone resorbing cells (osteoclasts). - The bone matrix is called osteoid and is formed of a type of collagen in which calcium salts are deposited. - **Bone softening disease may be caused by:** - 1-Defective formation of osteoid eg. osteogenesis imperfecta. - 2-Defective mineralisation of osteoid e.g. Rickets. - 3-Increased resorption of bone by osteoclasts e.g. hyperparathyroidism. - 4-Decreased formation of bone by osteoblasts e.g. osteoporosis. ## Osteogenesis Imperfecta - It is a generalized mesenchymal disorder characterized by: - 1) Defective osteoid production causing failure of formation of mature bone. The bone formed is fragile resulting in multiple and repeated fractures. - 2) Defective collagen production resulting in ligamentous hyperlaxity of joints and blue sclera. - There are several types of the disease with variable degrees of affection: - 1) Congenital Type: - Still-born or born with multiple fractures. - 2) Infantile type: - They develop manifestations early in infancy by multiple easy fractures. - 3) Tarda type: - some cases develop manifestations in late childhood. - There is no specific treatment of the condition. - **Orthopedic management is directed to:** - Preventing fractures and deformities using plastic supporting devices. - Treating current fractures. - Correcting deformities which may need surgery. ## Rickets - It is a disease of growing bone due to inadequate calcification of bone matrix. - **Causes:** - **Infantile Rickets:** - Due to deficient intake of vitamin D and lack of exposure to sunlight, which is necessary for formation of vitamin D by the skin. - The disease manifests between 6 months and 3 years of age. - The other types of rickets are manifested in an older age. - **Coeliac Rickets:** - Due to deficient absorption of fat and vitamin D caused by hereditary intolerance to gluten. - **Renal rickets:** - Due to disturbed calcium phosphorus metabolism caused by renal dysfunction. - **Clinical Picture:** - The most important bony manifestations are bony deformities causing bow legs (genu varum) or knock knees (genu valgum). - **Characteristic signs of infantile rickets are:** - Boxy-bossy skull - Rickety rosary - Pigeon chest - Harrison Sulcus - Broad metaphysis - Marfan sign - **10 important clinical features in Rickets:** | Feature | Description | |:---|:---| | Delayed closure of fontanelles | | | Frontal bossing | | | Dental hypoplasia | | | Pectus carinatum | | | Swelling in wrist and ankle joints | | | Wide sutures | | | Craniotabes | | | Rachitic rosary | | | Harrison's sulcus | | | Bowing of legs | | - **X-ray:** - shows bone rarefaction (diminished density in x-ray). - The metaphyses become broadened and cupped and show brush border. - With healing the frayed brush border of the metaphysis becomes replaced by a line of calcified bone. - **Treatment:** - **Infantile rickets:** - Good diet rich in Ca, P and Vitamin D and exposure to sunlight as well as administration of vitamin D and calcium. - **Renal rickets:** - Needs administration of high doses of vitamin D in the form of active vitamin D (one alpha) and calcium. - Severe deformities not improving with medical treatment may need surgical correction(osteotomy). ## Hyperparathyroidism - Primary hyperparathyroidism results from increased secretion of parathyroid hormone by parathyroid hyperplasia or tumour. - This causes increased bone resorption by osteoclasts leading to: - 1) Hypercalcemia. - 2) Recurrent renal calculi. - 3) Bone resorption causes cystic changes in bones, bone deformities and pathological fractures. - Surgical treatment is by excision of parathyroid adenoma. ## Osteoporosis - It is diminished bone mass due to diminished bone formation by osteoblasts with aging and after menopause. - **Common sites affected are:** - **Vertebral column:** weakening of vertebrae. Causes vertebral collapse which causes back pain, kyphosis and gives a radiographic appearance of collapsed wedged or biconcave vertebra. - Proximal femur - Proximal humerus - Distal radius causing fracture after minor trauma. - **Diagnosis** is now possible using bone densitometry (DEXA). - **Treatment:** - 1) Adequate diet with good supply of calcium, vitamin D and proteins. - 2) Daily exercises and exposure to sunlight. - 3) Medications including: - Calcium, vitamin D - Calcitonin which increases osteoblastic activity - Bisphosphonates: Oral medications, which inhibit osteoclastic activity - Hormonal Replacement therapy (HRT) used in some cases.