Pathology Flashcards
Hepatitis
inflammtion of liver with three types
A: fecal/oral transmission of virus, water-borne infection
B: IV drug use and sexually transmitted, chronic carrier
C: former common cause of post-transfusion hepatits
Nutmeg liver
Chronic passive venous congestion
Seen in congestive heart failure
Cirrhosis
Chronic liver condition with damage fibrosis and regeneration nodules. presents with portal hypertension.
Caput medusae: diluted varicose veins radiating from umbilicus due to portal hypertension
Reyes syndrome
Rare cause of childhood hepatoencephalopathy caused by the use of aspirin in children with some illnesses
Chickenpox and influenza
Hepatocellular carcinoma
malignant hepatoma
Liver cancer associated with Hepatitis B and C, Cirrhosis, raised a-fetoprotein
associated with fungal aflatoxins
Painful hepatomegaly, anorexia, fatigue and weightloss
Pancreatitis
Inflammation of pancreas
Caused by alcohol, gallstones, trauma, steroids, mumps and hypercalcemia
swollen pancreas and leaking enzymes
abdominal pain, blue discoloration (Cullen’s sign) around umbilicus or in the flanks (grey Turner’s)
Nausea, vomiting, and epigastric pain
Cholecystosis
Inflammation of gallbladder
Fair, fat, fertile, flatuent females over fourty
Right upper quadrant pain
Mostly caused by gallstones - most peopel wuth gallstones are asymptomatic
Pancreatic cancer
Malignancy arise from pancreatic duct
Painless juandice, clay colored stool if the cancer is in the head of the pancreas
Weight loss due to malabsorption and anorexia
Poor prognosis
Osteoporosis
Loss of bone quality while bone quality is normal
more commpn in post-menopausal women
Senile type is due to lack of growth hormone and more common in older men
Osteomalacia
Loss of bone quality with softening of the bone
Decreased vitamin D in adults
Looser’s zone on x-rays of long bones
Rickets
Loss of bone quality
Decreased vitamin D in children
Bowlegs and rachitic rosary
Osteitis fibrosa cystica
Due to hyperparathyroidism
Brown bone cysts
Paget’s disease
Osteitis deformans
Possible paramyxovirus infection
Older people with thickening of bones and deformitis
Achondroplasia
Autosomal dominant
Short limbs with normal head and trunk
Charcot’s joint
Neuropathic joint disease: joint destruction because of loss of pain
Caused by: tabes dorsalis, diabetes mellitus, syringomyelia, leprosy, leprosy
Osteogenesis Imperfecta
Autosomal dominant
Brittle bone disease
Blue sclera
defective collagen synthesis
Osteomyelitis
Blood borne infection
S. aureus is the most common
Salmonella organisms in Sickle Cell Disease
P. organsims in intravenous drug users
Osteochondroma
Bone outgrowth
Capped by cartilage
Echondroma
Most common benign tumor in hand
Expansile benign cartilage tumor in bone
Ollier’s disease
Multiple enchondroma
Osteoma
Dense mature bone insland in the skull or spine
Giant Cell Tumor
Benign metaphyseal bone tumor extending into the epiphysis
Aneurysmal Bone Cyst
Eccentric soap bubble x-ray appearance extending from diaphysis into metaphysis
Multiple myeloma
Most common primary bone cancer after 50 years. Nosturnal bone or back pain, recurrent infection, hypercalcemia
Punched out lesions
Raised IgG causing an M spike on serum electrophoresis
Bence Jones proteins in urine
Osteosarcoma
Second most common malignant bone tumor - most common in teenagers
Seen in patients with Paget’s disease
Codman’s triangle of periosteal elevaton on x-ray
Chondrosarcoma
3rd most common bone tumor in men 30-60
Ewing’s sarcoma
Malignant tumor mimicking osteomyelitis
Onion skin appearance on x-ray
Rheumatid arthritis
autoimmune biulateral small joint disease in HlA-DR4 positive patients
Rheumatoid factor 9IgG) in 70-80% of pts
Pannus formation: Inflamed granulation tissue in the joint space destroying articular surface
swan neck, ulnar deviation, boutonniere, metacarpophalangeal joint swelling, proximal interphalangeal joints
Still’s disease
juvenile Rheumatoid Arthritis
Affects small and medium size joint pains mainly wrist and knee lymphadenopathy and splenomegaly in kids and teens
Sjorgen’s syndrome
Dry eyes, mouth and arthritis
seen in RA and scleroderma
Sommon in women 40-60
SS-A and SS-B antibodies
Felty’s syndrome
Splenomegaly
Neutropenia
Seen in patients with RA
Systemic Lupus Erythematosus
Unknown
Autoimmune disorder: antinuclear antibodies, anti-ds DNA antibodies
More common in younger (black) females
Multiple organ system
Seronegative arthritis
Rheumatoid factor is negative
HLA-B27 is positive
Reiter’s syndrome, Psoriatic arthritis, Ankylosing Spondylitis
Psoriatic arthritis
Polyarthritis with silvery scales over extensor aspects
Autoimmune disorder causing rapid turnover of skin
Pitted nails and dactylitis
HLA-B27 + arthritis pair
Ankylosing spondylitis
Sacroiliitis and low back pain
Bamboo spine and a positive HLA B27 genetic marker
Inflammatory Bowel Disease (like ulcerative colitis)
Some patients with uc present with joint pains
Reiter’s syndrome
(can’t pee, can’t see, can’t dance with me)
Urethritis
Arthritis - Joint or heel pain
Conjunctivitis
caused by chlamydia or shigella infection
Osteoarthritis
Degenerative disease affecting weight bearing joints
Causes subchondral sclerosis, osteophytes, Heberden’s and Bouchard’s nodes
H nodes: Primary osteoarthiritis in distal interphalangeal joints of fingers (females)
B nodes: swelling of proximal interphalangeal joints in OA and RA
Gout
Podagra (affects foot) gonagra (affects knee)
due to hyperuricemia
common in males and associated with alcohol and purine-rich foods
Alcohol metabolites compete for xcretion from the kidney at the same site as Uric acid
Acute: 1st metatarsophalangeal joint pain
Chronic: characterized by tophi - accumulation of uric acid crystals in the ear and skin over joint
Lyme disease
Caused by Borrelia burgdorferi
transmitted by tick
Polyarthritis with bulls-eye lesion
(polyarthritis, extra-articular)
Myasthenia gravis
Acteylcholine receptor antibodies
Major peak incidence in 30+ yo females; second peak in 60+ yo males
Diplopia, ptosis, problems with chewing, fatigue with repetitive muscle use
Tensilon test is positive
80% of females myasthenia pts have thymic pathology (65% have thymic hyperplasia; 15% have a thymic tumor)
Lambert-Eaton syndrome
Auto-antibodies to the pre-synaptic voltage-gated Ca channels in the NM junction
Prevents acetylcholine from being released by the vesicles
Seen in small (oat) cell lung cancers
Older male population
Weakness improves with repetitive use
Tension test is usually negative
Dermatomyositis
unknown cause, common in females
Autoimmune disorder
Heliotrope rash (reddish purple eyelids and papules on knuckles)
Produces anti-nuclear antibodies
associated with malignancies of lung, breast, ovary, gut
Duchenne’s muscular dystrophy
sex-linked recessive
absence of dystrophin
predominantly males
Pseudohypertrophic calves - Muscle infiltrated by fat and connective tissue. Muscle appears big and strong but is weak.
Death from cardiorespiratory failure before 20
Becker’s muscular dystrophy
sex-linked recessive
Inadequate dystrophin levels
Not as severe as Duchenne’s and live 40+ years
Charcot-Marie-Tooth disease
Progressive hereditary nerve damage
Peroneal muscular wasting
Inability to evert the foot
Leg-Calve-Perthes disease
Ischemia and subsequent avascular necrosis of the head of the femur
Unknown cause
More common in young boys
Slipped capital femoral epiphysis
Displacement of epiphysis of the head of the femur
More common in overweight children and teens
Possible traumatic Salter-Harris type 1 epiphyseal fracture
Polymyalgia rheumatica
unknown cause older females > 50 years Pain and stiffness in shoulder and hips Malaise and fever Associated with temporalis arteritis May lead to blindness Highly elevated ESR with normal creatine kinase
Spina bifida
Neural tube defect due to B9 deficiency in the first trimester. Associated with elevated levels of alpha-feraprotein
- occulta presents with failure of neural arch to close and with a tuft of hair over a dimple in the lumbar spine region
- vera is a more severe form with failure of neural arch to close with meningeal herniation under the skin.
Meningocele
Protrusion of meninges through defect in the spinal column
Myomeningocele
A protrusion of meninges and spinal cord through spinal column defect
Anencephaly
Failure of brain and spinal column to develop
Hydrocephalus
Accumulation of excessive CSF in the ventricles
Obstructive - Caused by obstruction of flow of CSF: non-communicating type
Reversible cause of dementia
incontinence, ataxia, dementia
Arnold-Chiari deformity
Small posterior fossa with cerebellar herniation into the foramen magnum
Type-1: cerebellar tonsils into foramen magnum
Type-2: C vermis and medulla into the f magnum
Dandy-Walker syndrome
Large posterior fossa
Cystic dilation of the 4th ventricle
Cerebral Palsy
Non-progressive motor disorder due to prenatal brain anoxia
Scissors gait is seen with UMN lesion of CP
Subdural hematoma
Accumulation of blood under dura
tear of dural veins and may be a result of trauma in the elderly
Extradural hematoma
Accumulation of blood outside of the dura
Trauma in adults: meningeal artery tear
Subarachnoid hemorrhage
Accumulation of blood under the arachnoid
May be due to ruptured berry aneurysm: saccular congenital swelling in a cerebral artery. Increased incidence in adult polycystic disease of the kidney
Cerebrovascular accident
stroke
Sudden CONTRALATERAL motor/sensory loss due to interrupted blood supply to the brain.
Transient Ischemic Attacks are similar but are brief episodes of dysfunction caused by small emboli lasting less than 24 hours
Thrombosis vs. embolism
T: clot formed in atherosclerotic blood vessel
E: mass of undissolved material in blood vessel brought by the blood
Intracerebral hemorrhage
Accumulation of blood inside the brain
Meningitis causes
N. meningitidis, E. coli, H. Influenza