Reproductive, Musculoskeletal, and CNS Ah 120 Fibrocystic Disease of the Breast Benign mixture of fibrotic, cystic lesions with ductal hyperplasia Caused by the stimulating effects of fluctuating estrogen levels Diagnosed by needle aspiration or surgical excision Treated by removing methylxanthines form diet and hormonal therapy eg, birth control pills Carcinoma of the Breast Most common malignancy in women over 30 Etiology Heredity Breast cancer genes BRCA1 and BRCA2 Menopause Especially with prolonged treatment with estrogen--progestin Pathology Adenocarcinoma replaces normal tissue in a glandular arrangement surrounded by connective tissue and fibrosis Because of proximity of axillary lymph nodes, it metastasizes early and easily Most often to lung or bone Signs & Symptoms Begins as a painless mass that eventually becomes palpable Also discharge from nipple or retraction of the nipple Distortion of the breast surface (mottling or orange-peel effect) Discoloration Ulcerative lesion on breast surface Diagnosis Breast self exam Needle biopsy Surgical excision with biopsy Ultrasound Fibrocystic Lesion Diagnosis (cont.) Normal Mammography Abnormal Treatment Surgery May be radical mastectomy with lymph node resection “Lumpectomy” with or without lymph node removal Chemotherapy and Radiation therapy May be done prior to surgery to shrink tumor Hormone Therapy Long term tamoxifen Endometriosis Presence of endometrial tissue outside of uterine lining Usually retrograde migration to ovary but may go anywhere in the abdominal cavity Endometriosis (cont.) Signs and symptoms vary throughout the menstrual cycle Abdominal and pelvic pain Excessive and abnormal bleeding Endometrial tissue is still influenced by hormones Infertility Treatment(s) Hormonal therapy Eg, birth control pills Pain meds Surgical excision of lesions that cause intractable pain Surgical excision may cause sterility Endometrial Carcinoma Adenocarcinoma of the uterus usually seen in post-menopausal women Endometrial Carcinoma (cont.) Etiology Irregular menstrual cycle history Infertility/no childbirth Delayed menopause Pathology Spreads through uterus, fallopian tubes, ovaries and out into peritoneal cavity Metastasizes via blood and lymphatic system Endometrial Carcinoma (cont.) Primary symptom is post-menopausal bleeding Diagnosis: Pap smear, D&C with biopsy Treatment: Hysterectomy with hormone therapy (usually progestin which increases the risk of breast cancer) and possibly chemotherapy Carcinoma of the Cervix Etiology Increased “wear and tear” on the cervix Promiscuity STDs Papilloma virus Maternal history of DES Pathology Spreads to adjacent structures (usually urethra/bladder and rectum) Metastasizes via lymphatics Carcinoma of the Cervix (cont.) Signs & Symptoms Abnormal bleeding Bladder & kidney infections (due to metastatic spread) Diagnosis Pap smear followed by colposcopy Carcinoma of the Cervix (cont.) Treatment Excision of the lesion Surgical (partial or total hysterectomy) Laser resection Cryocautery Freezing the lesion Radiation (may be done with implants) Ovarian Lesions Follicular (retention) cysts, adenomas, adenocarcinomas Follicular (Retention) Cyst Benign, nonneoplastic cyst May cause pain and possibility of rupture May cause internal hemorrhage Usually regress on their own without treatment Cystadenoma Benign, neoplastic cyst filled with serous fluid or mucus Can become very large and can be quite painful Treatment is usually surgical resection May require oophorectomy Cystadenocarcinoma Highly malignant adenocarcinoma May be primary or spread from endometrial carcinoma Usually no symptoms until it has metastasized Elevated CA125 Treated with aggressive surgery, chemotherapy, and radiation Prostatitis Inflammation usually caused by STD Can be acute or chronic Intense inflammation with abscesses Acute: swollen and squishy Chronic: swollen and hardened (because of fibrosis) Prostatitis (cont.) Signs & Symptoms: Dysuria and nocturia Low back pain Pyuria and leukocytosis May have fever if acute Signs and symptoms less severe if chronic Treated with antibiotics Benign Prostatic Hypertrophy (BPH) Enlargement of the prostate that usually starts at age 45-50 Caused by hormonal imbalance Increased dihydrotestosterone, a by-product of testosterone metabolization Causes obstruction of the urethra as it exits bladder BPH (cont). Signs & Symptoms Dysuria Difficulty in starting, stopping, and controlling urine flow May cause cystitis and pyelonephritis and complete urethral obstruction Treatment: Finasteride to inhibit dihydrotestosterone or surgery (TURP) Carcinoma of the Prostate Usually adenocarcinoma Very common in men over 50 Signs and symptoms are similar to BPH May also have hematuria S & S may not appear until it has metastasized to another location Carcinoma of the Prostate (cont.) Metastasizes throughout body, but preferentially to bone Diagnosed by: Digital exam Elevated PSA or acid phosphate in blood Transrectal ultrasound with needle biopsy Carcinoma of the Prostate: Treatment Surgery and /or radiation Surgery may damage nerves and result in impotence and incontinence For metatstatic spread – hormone therapy Removal of testosterone or addition of female sex hormones Testicular Carcinoma Most common in men under 30 Usual only symptom is a palpable mass through the scrotum on a testicle May metastasize via regional lymph nodes Treatment: orchiectomy May need chemo and radiation if cancer cells are found in lymph nodes Note: testicular cancer cells produce hormones that are seen in pregnancy. Thus a male with testicular cancer may have a positive pregnancy test! Musculoskeletal Diseases Bone Fracture Types Proper healing requires realignment and stabilization Stabilization may be done through external fixation (casts and splints) or internal fixation (surgical reduction with pins and rods) Abnormalities of the Vertebral Column Kyphosis –abnormal posterior curvature in upper back (“hunchback”) Caused by degenerative disease such as arthritis or by injury Abnormalities of the Vertebral Column (cont.) Lordosis – abnormal anterior curvature in the lower back (“swayback”) Caused by congenital defect, injury, muscular dystrophies, or poor posture Abnormalities of the Vertebral Column (cont.) Scoliosis – abnormal lateral curvature Due to congenital defect, poor posture, injury May compromise lung function Treated with exercises, physical manipulation, and in severe cases, surgery Herniated Nucleus Pulposus Herniation of disk material puts pressure on nerve roots Most common in lumbar spine) Caused by injury, or degenerative disease Causes pain and paresthesia on affected side and down affected leg Herniated Nucleus Pulposus (cont.) Diagnosed by myelogram, MRI, or CT Treatment: Rest, muscle relaxants, analgesics Manipulation Various surgical procedures Osteomyelitis inflammation of bone caused by infection Caused by staph or strep Skin lesions, compound fractures, orthopedic surgical procedures More common in children Damages medullary canal and weakens bone and makes it prone to further fracture and deformity Acute symptoms: bone pain and fever (may become chronic with minimal symptoms) Initially treated with antibiotics Osteoporosis decrease in bone density due to calcium loss Etiology: Aging, menopause, steroid therapy, immobilization, low dietary calcium Causes vertebral column abnormalities and increases the chances of fracture in weight bearing joints, eg hip and vertebral column Treated by:calcium supplements, vitamin D, and possibly hormone therapy Osteosarcoma Malignancy that develops in long bones Most common in the knee (distal portion of femur) More common in children Causes pain and limited range of motion Treated with chemotherapy followed by surgery Often metastasizes to lung Muscular Dystrophy Duchenne’s (most severe) and Becker’s (less severe) Inherited sex-linked recessive disease causing atrophy of muscle cells and replacement with fibrous and adipose tissue Causes postural abnormalities, difficulty with walking and eventually standing. May progress to affect the diaphragm and respiration Treatment is palliative Myasthenia Gravis A progressive loss of muscular strength with activity and then returns to normal after rest Is a descending weakness/paralysis Caused by an autoimmune reaction which damages the acetylcholine receptor site at the myoneural junction Treatment: Steroids and immunosuppressive drugs, plasmapheresis, thymectomy Osteoarthritis (Degenerative Arthritis) Degeneration of cartilage leading to roughening of the articular surface of bones Caused by aging and increased wear and tear Injury may lead to arthritis also Normal Knee Osteoarthritic Knee Osteoarthritis (cont.) Signs and symptoms: painful, swollen joints with limited range of motion Treatment: Exercises and physical therapy, pain meds, joint replacement, alternative treatments, ie, shark cartilage Rheumatoid Arthritis An autoimmune disease that affects ALL joints Usually starts in hands and feet Autoantibodies attack the synovial lining of joint capsules causing chronic damage and fibrosis Ankylosing (“fusing”) of joints eventually occurs Rheumatoid Arthritis (cont.) Signs and symptoms similar to osteoarthritis except that all joints become involved Patient may also develop skin nodules, lung fibrosis, and inflammation and vasculitis in the heart Treatment is similar to osteoarthritis Patients may also be put on methotrexate Central Nervous System Disease Cerebral Vascular Disease Atherosclerosis in circulatory system of the brain Often starts in the carotid arteries Risk factors are the same as for coronary artery disease (atherosclerosis in the coronary circulation) Smoking, obesity, high cholesterol, lack of exercise, high fat diet, hypertension, diabetes, age and heredity Transient Ischemic Attack (TIA) Transient ischemia caused by cerebral atherosclerosis that produces symptoms without causing permanent death of brain tissue A TIA is to the brain what angina pectoris is to the heart! Symptomology usually subsides within hours Cerebral Vascular Accident (CVA) Neurologic deficit due to severe and long lasting ischemia “STROKE” or “BRAIN ATTACK” Etiology of CVA Atherosclerosis leading to: Occlusion in a cerebral vessel due to thrombus or embolus and/or Vessels, brittle from atherosclerosis, or an aneurysm,rupture and hemorrhage CVA Pathology Brain cells die from lack of oxygen Like heart muscle, the dead cells are phagocytosed and replaced by scar tissue In CVA due to hemorrhage, additional damage is caused by the pressure buildup caused by accumulation of blood CVA Signs & Symptoms Change in LOC or loss of consciousness Loss of consciousness/coma most common with hemorrhagic CVA Hemiparesis Headache Unequal pupils Seizure (common in CVA caused by embolus) N&V Incontinence Speech disturbance Sensory disturbance CVA Diagnosis EEG, MRI, CT, Cerebral angiogram CT Scan Angiogram CVA Treatment Acute is like heart attack O2 and, if indicated, thrombolytics Hemorrhagic CVA may require craniotomy to control bleeding Physical therapy, Occupational therapy, Speech therapy Prevention Address risk factors for atherosclerosis Carotid Endarterectomy if indicated CVA Prognosis Approximately 30% recover without neurologic deficit Approximately 30% recover but have residual signs and symptoms due to neurologic deficit 30% die within 6 months CVA For many, primary residual effect is seizure disorder (Epilepsy) Neurologic Deficit Central Nervous System Infectious Diseases Meningitis Infectious inflammation of the meninges (the 3 layered membrane that surrounds the brain and spinal cord) Etiology: Bacterial: Meningococcus (Neisseria menigitidis) and Pneumococcus (Streptococcus pneumoniae) Meningococcus is most contagious Viral Meningitis: usually not as severe as bacterial Meningitis: Pathology Yellow-pus exudate forms in the meninges around the brain and spinal cord Causes brain dysfunction due to increased pressure Also interferes with drainage of CSF Meningitis: Signs and Symptoms Often URI manifestations first Headache Stiff neck and neck rigidity! Change in level of consciousness leading to complete loss of consciousness Patient often becomes combative and then lethargic prior to losing consciousness Still maintain neck rigidity even with loss of consciousness Hydrocephalus Meningitis: Diagnosis and Treatment Diagnosed by lumbar puncture Shows increased CSF pressure and appears cloudy because of presence of WBCs and infectious organism Treatment: Maintain airway and hydration, antibiotics for bacteria, possibly shunt for hydrocephalus Meningitis: Complications Epilepsy Hydrocephalus Hearing loss Learning disability Brain Abscess Bacteria or parasite, eg, tapeworm, that migrates from original site of infection to brain and causes intense inflammation with abscess formation Usually diagnosed by MRI or CT scan Brain Abscess (cont.) Signs and Symptoms: Depends on location in brain Headache, seizures, personality changes, memory loss, motor and/or sensory disruption Treatment: Antibiotic/Antiparasitic drugs and surgical drainage of the abscess Encephalitis Inflammation of the brain, meninges, and spinal cord Usually caused by a virus: herpes simplex, HIV, arboviruses (carried by mosquitoes), rabies TB can also cause encephalitis “Sleeping Sickness” Encephalitis (cont.) Signs and Symptoms: Fever, headache, agitation and delirium, seizures, coma/catatonic state Diagnosis: Lumbar Puncture shows cloudy CSF with increased WBCs Treatment: Supportive Prognosis: High mortality and recovery usually includes residual neurologic deficit Myelitis Inflammation of the spinal cord, usually due to a virus Eg, Poliovirus Causes inflammation in the anterior horn cells of the spinal cord causing varying degrees of weakness and paralysis The higher up in the spinal cord the inflammation, the more complete the paralysis is Myelitis (cont.) Often spread through contaminated water Virus matures in the GI tract before attacking the spinal cord Very contagious since it is freely shed in saliva and fecal material Treatment: Prevention! Polio vaccine Acute case requires supportive care often requiring mechanical ventilation Recovery can be slow and there is often residual muscle weakness and atrophy Guillain-Barre’ Syndrome Idiopathic Polyneuritis Widespread acute demyelination of peripheral nerves and nerve roots with some axon degeneration Causes an “ascending” weakness/paralysis that may last days, weeks, or months Can not predict how severe, high up, or long the condition will persist Worst cases progress to complete paralysis with respiratory failure due to diaphragmatic paralysis Guillain-Barre’ (cont.) Etiology: usually a complication of a viral infection or viral vaccine Viral activity is believed to trigger an autoimmune reaction to myelin Signs and Symptoms: varying degree of weakness/paralysis that starts in the legs and works its way up Treatment: Supportive including mechanical ventilation and physical therapy Patients may experience residual weakness and muscle atrophy after recovery Herpes Zoster (Shingles) Viral infection of peripheral dermatomes that causes painful, erythematous, vesicular lesions Believed to be caused by dormant varicella Herpes Zoster (cont.) Outbreak can be triggered by stress, malnutrition, drug reaction, or another viral illness Virus appears to be opportunistic (as are all Herpes viruses) Can be very contagious while lesions are still “wet” Treatment: Steroids (topical and systemic) After eruption clears, patient may be troubled by pain at site for weeks or months CNS Degenerative Diseases Multiple Sclerosis A chronic disease, with periods of remission and exacerbation, characterized by diffuse, focal areas of degeneration of the myelin sheath of nerve fibers in the brain and spinal cord Result is build up of scar tissue (sclerosis) MS (cont.) Etiology: Believed to be an autoimmune reaction that MAY be triggered by a viral infection Is more common in colder climates Heredity also a factor Diagnosed by MRI MS (cont.) Signs and Symptoms (depend on where the demyelination is occurring): Usually develops between ages 15-40 and may include: Paresthesia, weakness, visual problems, ataxia, tremors, incontinence, with progression to total paralysis Periods of remission and exacerbation Treatment:Primarily supportive with physical therapy Life span usually 25 years after diagnosis Parkinson’s Disease Degeneration of the substantia nigra in the midbrain causing decreased amounts of dopamine Lewy bodies are seen in degenerating substantia nigra Very common after age 50 Parkinson’s (cont.) Signs and Symptoms (caused by dopamine deficiency): Resting tremors, masklike expression, muscle rigidity, shuffling gait, monotone speech, possibly dementia Treatment: L-dopa, implanted substantia nigra cells, electrical stimulation of midbrain, stem cells(?) Alzheimer’s Disease The most common form of senile dementia Degeneration and atrophy in the cerebral cortex with formation of neurofibrillary tangles and senile plaques Results in memory loss and deterioration of intellectual functions Alzheimer’s (cont.) Exact etiology unknown Heredity, Down’s Syndrome, viral infection, betaamyloid (cause or manifestation?), A-beta star Signs and Symptoms - 3 Stages: Stage 1 – memory loss, poor judgement and reasoning, spatial and temporal disorientation, apathy and paranoia Stage 2 – aphasia, agnosia, incontinence, continued deterioration of cognitive function Stage 3 – severe impairment of all cognitive and motor functions Treatment: Memory stimulating drugs such as donepezil (Aricept) and tacrine (Cognex) Brain Cancer Most are secondary tumors that have metastasized from elsewhere in the body Most commonly from lung, breast, colon, bone, or melanomas Brain Cancer (cont.) Primary tumors may arise from the meninges, ie meningioma, which is benign but may put put pressure on the spinal cord or brain Other primary tumor is a glioma which is always malignant astrocytoma and glioblastoma multiforme Brain Cancer (cont.) Signs Symptoms depend on what part of the brain the tumor is in and are usually due to the increase in intracranial pressure caused by the tumor Headache, N &V, seizures, memory loss, cognitive dysfunction, personality change, motor and/or sensory dysfunction, increased CSF pressure during lumbar puncture Brain Cancer (cont.) Diagnosed by CT scan and/or MRI Treatment: Surgical resection (if possible) Surgery may actually make patient worse! Chemotherapy and radiation therapy Epilepsy A condition of RECURRENT seizures. Seizure A sudden, transient alteration in electrical activity in the brain which may cause sensory, motor, and psychic symptoms as well as impairment of consciousness Seizure Etiology Hypoxia Toxins High temperature (febrile) Electrolyte imbalance Hypoglycemia Sleep deprivation Brain lesions Neoplasm, abscess, trauma, infection, CVA, congenital lesions Besides causing a seizure, any of these conditions could make injured brain tissue become epileptogenic. However,many cases of epilepsy are idiopathic! Epilepsy: Seizure Triggers Excitation, relaxation, falling asleep, waking up Sounds, flashing lights Hyperventilation, drugs/alcohol, stress, sleep deprivation Epilepsy: Seizure Types Partial – abnormal electrical discharge is confined to a limited area of the brain at the onset of the seizure Simple partial – no impairment of consciousness. Symptoms depend on area of brain involved Complex partial –may have some impairment of consciousness. Obvious sensory and/or motor symptoms May exhibit “automatisms’ Epilepsy: Seizure Types Generalized – abnormal electrical activity occurs throughout brain causing loss of consciousness Absence’ (petit mal) Common in children Brief attacks lasting 5-30 seconds Blank stare , eyes may blink rapidly Some loss of muscular tone Patient is unaware and functions normally after seizure Often initially diagnosed as a learning disability Epilepsy: Seizure Types Generalized (cont.) Tonic – Clonic (grand mal) Tonic phase Loss of consciousness with tonic stiffening of all muscles Patient does not breathe and gets cyanotic Tonic phase may last 1 minute Clonic phase – synchronized jerking of extremities and head Intense salivation and tongue biting May last 1-4 minutes Post –Ictal phase Patient is drowsy and confused May experience N & V and incontinence Treatment During Tonic-Clonic Tonic phase – help patient down to prevent them from hitting their head Do NOT force anything in their mouth! Clonic phase – move things out of their way or put pads around them May lay on side if jerking is not too intense Do not try to restrain or try to force anything in their mouth Post – Ictal – open and clear airway and assist patient as needed Epilepsy: Diagnosis Besides seizure history, the definitive diagnosis is made by an EEG Normal May use strobe lights or hyperventilation Tonic-Clonic Epilepsy: Treatment Anticonvulsants to prevent seizures Zarontin for absence’ seizures Tegretol, Depakote During a seizure, IV Valium may be given to put patient in post-ictal phase Surgery if epileptogenic tissue can be identified and is accessible Correct problems causing development of epileptogenic tissue Sample Test Questions! An infection with a bacteria that causes yellow pus to surround the brain and spinal cord is: A. Encephalitis B. Rabies C. Guillain-Barre’ syndrome D. Meningitis E. Thyroiditis A small percentage of patients with rheumatoid arthritis may develop: A. Inflammation of the lung B. Skin lesions C. Brain tumors D. Tetany E. A and B Methods used to diagnose CVA include: I. CT scan II. MRI III. Angiography IV. EEG A. I only B. I and II C. II and III D. II and IV E. I, II, III, and IV A compound fracture is defined as: A. A breakage of two or more bones in close proximity B. A breakage of a bone in two or more areas C. A breakage of a bone so that an end protrudes through the skin D. A breakage of bone producing several slivers of bone E. B and C Women who never had children and develop cancer after menopause usually have which cancer? A. Endometrial adenocarcinoma B. Endometrial squamous carcinoma C. Cervical adenocarcinoma D. Cervical squamous carcinoma E. Fibroadenoma If metastasis of breast cancer occurs, what two areas are most commonly involved? A. Lung and heart B. Liver and spleen C. Lung and bone D. Ovaries and uterus E. Prostate and testes A malignant tumor that originates in the brain is most likely a: A. Meningioma B. Cerebral sarcoma C. Glioma D. Encephalocarcinoma E. Brainoma A disease of the joints which spreads to all joints causing permanent deformity and ankylosing is: A. Osteoarthritis B. Osteoporosis C. Rheumatoid arthritis D. Degenerative arthritis E. Osteomyelitis