Kaplan Qbank Flashcards
Parasite assoc w/
Megacolon, Megaesophagus,
+ Dilated Cardiomyopathy
Chagas Disease
(Intracellular protozoan parasite Tripanozoma Cruzi)
Transmitted via Reduviid bug bite in South America.
Rx: Nifurtimox
Parasite assoc w/
Bladder
Schistosoma Haematobium
Predisposes Squamous Cell Carcinoma of Bladder
Brain Parasite assoc w/
HIV
Toxoplasma Gondii
2 Brain Parasites assoc w/
Fresh water
Naegleria Fowleri
Acanthamoeba
Brain Parasite assoc w/
Dogs
Echinococcus Granulosis
2 Lung Parasites
Dirofilaria
Paragonimus Westermani
3 Small Intestinal Parasites
Ascaris
Taenia
Strongyloides
Granulosa Cell Tumor
ovarian follicle tumor
Solid + yellow ovarian mass, can produce estrogen.
Induces endometrial hyperplasia + higher risk of endometrial carcinoma.
Tumor cells have follicle-like structures, inhibin stains positive.
Dysgerminoma
ovarian cell tumor
Solid + tan ovarian mass, no hormone inbalance.
Clear cytoplasm + round/ovoid nuclei surrounded by abundant lymphocytic infiltrate.
+ Frec in mosaic Turner Sd + Pseudohermaphroditism.
Krukenberg Tumor (ovarian MTS tumor)
MTS gastric signet-ring carcinoma to ovary
Assoc w/ endometrial hyperplasia + uterine bleeding
ADPKD
(Autosomal Dominant
Polycystic Kidney Disease)
Progressive renal failure, hematuria, HTN, renal stones, cysts in kidneys + liver.
Mutation in PKD1 + PKD2 genes, onset 50s.
Assoc w/ berry aneurysms in circle of willis (ACA + PCA)
ARPKD
(Autosomal Recessive
Polycystic Kidney Disease)
Infantile ADPKD: earlier onset + more severe sympt
CAH
Congenital Adrenal Hyperplasia
21-Hydroxylase Def
Baby girl w/ ambiguous genitalia, vomiting, dehydration.
Aldosterone def (Hypo Na+, Hypo Cl-, Hyper K+) Cortisol def (hypoglycemia) Elevated 17-Hydroxyprogesterone, DHEA, Androstenedione, Renin.
Klinefelter Sd
XXY
Tall, small penis + testes, infertility, gynecomastia, sparse body hair.
Abnormal clumped Leydig cells
Low Testosterone.
High GnRH, LH, FSH.
4 Tumors w/ Psamomma Bodies
dystrophic calcifications
Necrosis cluster w/ crystallization of Ca+ salts
. Papillary Carcinoma of Thyroid
. Serous Papillary Cystadenocarcinoma of Ovary
. Meningioma
. Malignant Mesothelioma
Acetaminophen Toxicity Labs
Acute Liver injury
. Elevated AST, ALT (hepatocytes)
. Normal ALP (bile duct + billiary tree)
. Normal Amylase (pancreatitis)
Obesity Hypoventilation Sd (OHS)
Pickwickian Sd
Chronic alveolar hypoventilation assoc w/ obesity
> 90% have OSA (Obstructive Sleep Apnea)
Chronic respi acidosis w/ metab compensation, RVH
Rx is CPAP + weight loss
Osmotic Demyelination Sd (ODS)
Central Pontine Myelinosis
Rapid correction (>8 mEq/d) of hypoNa+ (<120 mEq/L) after 2-3 days of adaptation can lead to demyelinating axons in central pons + Locked-In Sd.
Surreptitious Thyroxine Dosing
Hyperthyroid condition (increased T4) and decreased Iodine uptake, suspect exogenous thyroxine. Endogenous hyperthyroidism would have increased Iodine uptake as well as increased T4..
(Oculomotor) CN3 Compression
CN3 (Oculomotor) nerve passes b/t sup + inf cerebellar artery (by basilar artery)
An aneurysm + compression of CN3 leads to loss of adduction of that eye.
Long Thoracic Nerve Lesion
Nerve that innervates Serratus Anterior musc.
Lesion leads to winged scapula.
Axillary Nerve Lesion
Nerve that innervates Teres Minor + Deltoid musc.
Lesion leads to arm abduction weakness.
Dorsal Scapular Nerve Lesion
Nerve that innervates Rhomboideus Major + Minor musc.
Lesion leads to minor winging of scapula.
Suprascapular Nerve Lesion
Nerve that innervates Supraspinatus + Infraspinatus musc.
Lesion leads to difficulty elevating arm.
(ARDS) Acute Respi Distress Sd
Def + Dx
Non-cardiogenic pulmonary edema
Triggered by trauma, mult transfusions, pancreatitis
Onset several hrs after trigger
Dx via ABG (decreased PaO2/FiO2 ratio <200 mmHg)
Enzyme Def in:
Albinism (Classic AD form)
Tyrosinase Def
Aromatic AA Tyrosine cannot be converted to melanin in melanocytes, increasing risk of sunburn + skin cancer.
Enzyme Def in:
Maple Syrup Urine Disease
Alpha-Ketoacid Dehydrogenase Def
Branched-chain AA (alpha-ketoacids) cannot be metabolized and accumulate in blood, leading to metab ketoacidosis, motor prob + seizures, urine smell of maple syrup or burned sugar.
Enzyme Def in:
Tay-Sachs Disease (AR)
Hexosaminidase A Def
Glycolipid disorder leads to accumulation of Ganglioside GM2 in neurons, cherry-red macula in retina, blindness, loss of developmental milestones, death before 5yrs.
Enzyme Def in: Hunter Disease (X-Linked)
Iduronate 2-Sulfatase Def
Glycoprotein disorder leads to accumulation of Heparan + Dermatan Sulfate in urine, retardation, coarse facial features, hepatosplenomegaly, cardiac defects, clear corneas, short stature, hearing loss.
Severe form is lethal by 5yrs.
Enzyme Def in:
Homocystinuria (AR)
Cystathionine Beta Synthase Def
Methionine cannot be produced, leading to accumulation of sulfur-containing AA Homocysteine.
Looks like Marfan, limited joint mobity, retard (severe form), increased risk of thrombosis (DVT, MI, Stroke) by 30s-40s.
Translocation in:
t(14;18)(q32;q21)
Follicular B Cell Lymphoma - t(14;18)(q32;q21)
Xs 14 site involves Ig heavy chain locus (IgH)
Xs 18 site involves Bcl-2 oncogene
Translocation produces hybrid Bcl-2/IgH transcript
Bcl-2 inhibits apoptosis, so this raises cancer risk!
Translocation in:
t(11;14)(q13;q32)
Mantle Cell Lymphoma (MCL) (+ Mult. Myeloma)
t(11;14)(q13;q32)
Xs 11 site involves Bcl-1 oncogene
Xs 14 site involves Ig heavy chain locus (IgH)
Translocation produces hybrid Bcl-1/IgH transcript
Translocation in:
t(12;21)
Acute Lymphoblastic Leukemia (ALL) -t(12;21)
Favorable Px in kids
Translocation in:
t(9;22)
Chronic Myelogenous Leukemia (CML) -t(9;22)
Poor Px + adult presentation in:
Acute Lymphoblastic Leukemia (ALL)
Translocation in:
t(15;17)
Acute Myelogenous Leukemia (AML) -t(15;17) Promyelocytic type (APL)
Translocation in:
t(8;14) Or t(2;8) Or t(8;22)
Burkitt Lymphoma
t(8;14) -> hybrid myc/IgH transcript
t(2;8) -> hybrid kappa Ig light chain/myc transcript
t(8;22) -> hybrid myc/lambda Ig light chain transcript
Esophagus path:
Mallory-Weiss Tears
Lesions in Esophagus Mucosa
Caused by frequent vomiting (acute/chronic OH, bulimia)
Mild Upper GI bleeding
Esophagus path:
Boerhaave Sd
Esophagus tears through all layers!
Causes fluid/air in mediastinum (Pneumomediastinum)
Assoc w/ forceful vomiting, chest pain, pain on swallowing
Esophagus path:
Esophageal carcinoma
Either Adenocarcinoma or Squamous Cell Carcinoma
Onset as progressive dysphagia, not acute bleeding
Esophagus path:
Achalasia
Motor dysfunction of Lower Esophageal Sphincter (LES)
Difficulty swallowing, accumulation of food leads to dilation + megaesophagus, bleeding uncommon
Dx barium swallow with “Bird Beak” appearance
Esophagus path:
Schatzki Rings
Benign mucosal rings at Esophagus squamocolumnar junction (below Aortic arch)
Caused by chronic GERD
Esophagus path:
Zenker Diverticulum
Evagination of Esophagus at Pharynx junction
Causes dysphagia + halitosis, not bleeding
Esophagus path:
Esophageal Varices
Dilated + tortuous Submucosal Esophageal veins
Develop secondary to Portal HTN, after cirrhosis
+frec causes of cirrhosis (chronic OH, HCV)
Onset as life-threatening bleeding, no prior vomiting
Plummer-Vinson Sd
. Hypochromic + Microcytic Anemia
. Esophageal webs
. Atrophic glossitis
2 Phases of Salicylate Poisoning
1. Acute Respi Alkalosis (high pH, low PCO2, near normal HCO3) 2. [12-24hrs later] Metabolic Acidosis (lactic acidosis -> metab acidosis with low HCO3) Also assoc w/ Tinnitus, N+V, Fever
Acetaminophen Poisoning
Symptoms + Rx
N+V, Abdominal pain, Hepatic Failure
Rx: N-Acetylcysteine within 8hrs prevents hepatic failure
Hydrochlorothiazide Poisoning
Symptoms
Metabolic Alkalosis (via H+ excretion) [HyperGLUC] HyperGlycemia HyperlLipidemia HyperUricemia HyperCa+
Chronic Lead Poisoning
Symptoms
. Sideroblastic anemia (Basophilic stippling of RBCs)
. Neuropathy
. Kidney Dysfunction
. Abdominal pain
Chronic Mercury Poisoning
Symptoms
. CNS atrophy
. Gingivitis
. Gastritis
. Renal Tubular changes
Acute Mercury Poisoning
Symptoms
. GI Epithelium Necrosis
. Renal Tubular Necrosis
Sheehan Sd
Postpartum hemorrhage leads to hypopituitarism
Rx: Glucocorticoids + Thyroxine asap
How to Calculate
Serum Anion Gap?
Use? Normal Range?
Anion Gap = (Na+) - (HCO3 + Cl+)
. Used to determine b/t causes of Metabolic Acidosis
. Normal Range (8-16 mEq/L)
2 Causes of Metabolic Acidosis
w/ Elevated Anion Gap
. DM + Ketoacidosis
. Shock/HF + Lactic Acidosis
2 Causes of Metabolic Acidosis
w/ Normal Anion Gap
. Diarrhea + Loss of HCO3 (also K+)
. Renal Tubular Acidosis + Retention of H+
Primary Hypothyroidism
Lab Values
Thyroid Gland Problem:
. Elevated TRH, TSH
. Low T3, T4
Secondary Hypothyroidism
Lab Values
Anterior Pituitary Problem:
. Elevated TRH
. Low TSH, T3, T4