Wednesday, December 28, 2005
Tuesday, December 13, 2005
Tuesday, November 29, 2005
History and Physical for Pulmonary Embolism
Chief Complaint | ||||||||||||
chest pain and shortness of breath | ||||||||||||
History of Present Illness | ||||||||||||
23 year old female with past medical history significant for birth control use of five years and 15 smoke pack years presents witch chest pain and shortness of breath. Four days prior to admission, she started to experience a dull, substernal pain with deep breaths. Two days prior to admission, she experienced shar pain in lower left anterior axillary line with deep breaths. One day prior to admission, she started to experience upper left sided chest pain. While at her Ob-Gyn office on the morning of admission, she was experiencing shortness of breath, and she was told to go to the ER. Currently, her chest pain is constant on the left side. She says she can walk ten steps before becoming short of breath. She denies palpitations, leg pain, nausea, vomiting, diarrhea, cough, pain radiation. Previously, she experienced chest pain during this current summer which went away in four days without hospital admission. | ||||||||||||
Past Medical History | ||||||||||||
Patient denies hypertension, diabetes, stroke, coronary artery disease, rheumatic fever, asthma, or spontaneous abortions. Patient has been on Depo-provera for five years prior to current birth control of Norgestrel. | ||||||||||||
Past Surgical History | ||||||||||||
Patien did not have previous surgeries. | ||||||||||||
Medications | ||||||||||||
Norgestrel Unisom | ||||||||||||
Immunizations | ||||||||||||
Patient has not received her pneumococcal, hepatitis, or flu vaccine. | ||||||||||||
Allergies | ||||||||||||
NKDA | ||||||||||||
Family History | ||||||||||||
Father is alive, 52 years old without hypertension, diabetes, coagulopathy, or coronary artery disease. Mother is alive, 46 years old. She has hypertension. She has no history of coronary artery disease, coagulopathy, or diabetes.Both grandmothers had strokes at old ages. Her family has no history of cancer or coagulopathy. | ||||||||||||
Social History | ||||||||||||
Alcohol - She drinks up to 12 beers during the weekend over one to two nights. Tobacco - She has been smoking 1.5 packs per day for 10 years Substance - She denies any substance abuse. Psychosocial - She denies any changes in her general behavior. She lives with her friend after leaving her family residence. Functional - She believes she has normal function. | ||||||||||||
Review of Systems | ||||||||||||
General: () weight loss () fever () night sweats () weakness/fatigue () appetiteEndocrine: () heat intolerance () decreased energy () thyroid/reanl dz () polydipsia () polyuriaLympatics: () lymphadenopathySkin: () itching () pale () palmar creases Hematology: () anemia () bruising () bleedingHead: () seizures () trauma () loss of conscioussness () headache () vertigo () dizzinessEyes: () visual changes (X) blurred vision () loss of vision () dischargeEars: () discharge () ear pain () tinnitus () ototoxic drug history () hearing lossNose: () discharge () rhinorrhea () epistaxisMouth and Throat: () lip cracking () gum soreness () gum hypertrophy () dryness () thirst () excessive salivation () throat pain () hoarsenessCardiorespiratory: (X) SOB () valvular disease (X) orthopnea (X) dyspnea on exertion () nocturia () edema (X) paroxysmal nocturnal dyspnea () cough () cyanosis () hemoptysisGastrointestinal () dysphagia () abdominal pain () vomiting () hematemesis () melena () hematochezia () change in appetite () diarrhea () constipation () jaundiceGenitourinary: () change in bladder function () change in amount () dysuria () hematuria () dischargeNeuropsychiatric: () weakness () motor/sensory deficit () depression () anxietyPain: Chest pain on left side | ||||||||||||
Physical Exam | ||||||||||||
General Appearance:Vital Signs:Temperature: 98.1 F Oxygen Saturation: 100% on RA Blood Pressure: 125/82 Respiratory Rate: 18 Pulse Rate: 117Skin/Nails:Head:Eyes:Ears:Nose:Throat/Mouth:Neck:Lymph:Pulmonary: CV:Abdomen:Breasts:Rectal:Genitals:Peripheral pulses:Musculoskeletal:Neurologic:Mental StatusCN ICN IICN III,IV, VI CN V, VIICN VIICN VIIICN IX, XCN XICN XIICerebellarDTRs | ||||||||||||
Labs | ||||||||||||
Troponin I <0.05,>D-Dimer 3.20 Imaging CT - Multiple pulmonary embolisms on the right upper lobe, right lower lobe, left upper lobe, and left lower lobe in the segmental and subsegmental branches. Her right middle lobe does not have a pulmonary embolism.
| ||||||||||||
Assessment/Plan | ||||||||||||
23 year old female with a past medical history significant for smoking and contraceptive use presenting with multiple, acute pulmonary embolisms. She presented with some classic signs of pulmonary embolism including dyspnea and chest pain (1). 1. Tierney, Lawrence M., ed. Current Medical Diagnosis & Treatment. 44th ed. New York: McGraw Hill, 2005. | ||||||||||||
Created with H and P |
Friday, November 25, 2005
Wednesday, November 23, 2005
Open CD 2.0
Provides free programs such as Open Office, Blender, Mozilla, GAIM, and others. Can be bought or downloaded for free.
Friday, November 18, 2005
Tuesday, November 08, 2005
Chronic Diarrhea
- Secretory Causes
- Medications
- Bowel Resection, Mucosal Disease, Enterocolic Fistula
- Hormones
- Carcinoid Tumor
- Serotonin
- Histamine
- Prostaglandins
- Kinins
- Gastrinoma
- VIPoma
- Calcitonin
- Somatostatinoma
- Carcinoid Tumor
- Congenital Defects in Ion Absorption
- Osmotic Causes
- Osmotic Laxatives
- Carbohydrate Malabsorption
- Steatorrheal Causes
- Pancreatic Exocrine Insufficiency
- Chronic Pancreatitis
- Cystic Fibrosis
- Pancreatic Duct Obstruction
- Chronic Pancreatitis
- Mucosal Malabsorption
- Tropical Sprue
- Whipple's Disease
- Abetalipoproteinemia
- Medications - colchicine, cholestyramine, neomycin
- Chronic Ischemia
- Tropical Sprue
- Postmucosal Lymphatic Obstruction
- Inflammatory Causes
- Idiopathic Inflammatory Bowel Disease
- Eosinophilic Gastroenteritis
Saturday, November 05, 2005
History and Physical for SOB
Age: 79 Sex: Male
CC: Chest pain, SOB for one day
Reason for Admission: Chest pain, SOB for one day
HPI: 79 yo AAM c right sided CP, not radiating, sharp, pleuritic, no aggravating or relieving factors. CP accompanied with SOB with acute to sub-acute onset. Pt has cough producing whitish sputum. He has chills, and currently, the patient is feeling better than last night.
PMH:
Sarcoidosis
COPD
PVD
DM
Glaucoma BL
Immunizations - he recieved his pneumo and flu vaccines last year.
PSH:
Fem-Pop bypass on left leg
Injuries/Disabilities: none
Medications:
Lovastatin 20 mg PO qday
Lasix 20 mg PO qday
Prednisone 5 mg PO qday
Lasix 40 mg PO qday PRN edema
Calcium 600 mg PO bid
Immunizations:
Pneumo and Flu received in 2004
Family History:
NA
Social History:
lives alone
past smoker for 50 years
past etoh
no IVDU
Review of Systems:
nausea, vomiting 2-3 times, no change in bowel movements, no dysuria
Physical Exam:
VS: Temp-101.5 BP-127/70 HR-90 Pulse Ox 80s in Er, currently went from 90 to 99, 101.5 degrees
Gen: mildly tachypnic, AO*3
HEENT: -JVD, carotid pulse- 2+ with no bruits, PERRL
Chest: CTA BL, -w/c/r
CVS: irregular rhythm, SEM II/VI
Abdomen: NT/ND, soft, +BS
Ext: -edema. -DP, Left calf tenderness
Neuro: no focal deficits present
Imaging:
CXR - Infiltrates R side and base
Labs:
Na - 140
K - 4.1
Cl - 101
CO2 - 29
BUN - 14
Cr - 1.0
Glucose - 137
Ca - 8.4
WBC - 11.4
HGB - 13.2
HCT - 39.3
PLT - 268
MCV - 81
EKG - freq PACs, LAD, Q waves in V2-V3, TWI in V1
CKMB - 1.3
Myoglobin - 142
Troponin - 0.05
Assessment:
79 yo AAM presented with intermittent SOB and chest pain on right side.
Problems List:
1. SOB
2. Chest pain
Differential Diagnosis:
1. COPD exacerbation - can present with cough, sputum production, and SOB.
2. Pulmonary Embolism - Pain in left calf could be a sign of a DVT and subsequent clot could have moved to the lungs. This could have caused the current symptoms of SOB and chest pain.
3. Pneumonia - CXR infiltrates, SOB, and chest pain can be from a community acquired pneumonia. Possible organisms include Streptococcus pneumoniae, Haemophilus influenza, Mycoplasma pneumoniae, Chlamydia pneumoniae, Staphylococcus aureus, Neisseria meningitidis, Moraxella catarhallis, and Klebsiella pneumoniae.
4. Sarcoidosis - a sarcoid inflammation of the lung can present with malaise, fever, and dyspnea. No hilar lymphadenopathy was present on CXR. No other findings of sarcoidosis were present: erythema nodosum, parotid gland enlargement, hepatosplenomegaly, and lymphadenopathy. Symptoms referable to other organs were not present either.
5. MI - a myocardial infarction can present with chest pain and SOB. The patient's location of pain on the right side, and lack of radiation make this less likely. His cardiac chemistry levels were well within normal limits.
Diagnostic Plan:
1. CT angio scan of chest
2. Pulmonary function tests
3. Pulse oximetry
4. Consult pulmonology
Therapeutic Plan
1. DVT prophylaxis
2. Heparin qtt
3. Antibiotics - Zithromax 500mg IV qday
4. O2 support 2L
5. Steroids
History and Physical for Sickle Cell Crisis
Informant: Patient - reliable
Age: 43
Sex: M
CC: pain in head, neck, arms, stomach, and legs
Reason for Admission: pain in head, neck, arms, stomach, and legs
History of Present Illness:
Patient 43 yo AAM presented with pain in arms, back, stomach and legs which started yesterday morning. His last crisis was 2-3 years ago. It is well localized to the areas mentioned. He tried using Percocet and Oxycontin but they were ineffective in controlling his pain. He also complains of a productive cough with yellow phlegm for 2-3 weeks. He had no associated chest pain. He had no nasal congestion, but he did have post nasal drip. He has no nausea, vomiting, diarrhea, fever or chills.
Past Medical History:
Sickle Cell Disease (SC) diagnosed at age 12. Not significant for any other chronic conditions such as diabetes or hypertension.
Past Surgical History:
No surgical history.
Injuries/Disabilities: Considers SC a disability.
Medications:
Oxycontin 80 mg po bid
Percocet 5 mg 1-2 tablets q 4-6 hours prn pain
Folic Acid 1mg po qday
Herbal Meds: none
Immunizations: Pneumo and flu vaccines up to date since last year
Allergies: hay
Drugs: Morphine - lack of coordination, nervous; toradol - lack of coordination
Food: none
Family History:
Mother has sickle cell disease and diabetes. His family has no history of hypertension, cancer, cardiac diseases, or thalassemia.
Social History:
He lives in an appartment with his fiance. He's currently unemployed due to his sickle cell disability. He has no history of alcohol abuse. He smokes 3-4 cigarettes per day.
Review of Systems:
Summary: - f/c, -n/v/d, -dysuria, + cough for 3 weeks, - rhinorrhea, - headache
Physical Exam
General Appearance: Pt in acute distress from pain
Vital Signs:
Temperature: 96.7 F Oxygen Saturation: 98% Room Air
Blood Pressure: 100/46
Respiratory Rate: 16 Pulse Rate: 68
Skin/Nails: no clubbing
HEENT: PERRL, clear nasal turbinates, non-erythematous pharynx, no thyroid enlargement, no lymphadenopathy
Pulmonary: CTA BL, -w/c/r
CV: S1S2, RRR, II/VI SEM
Abdomen: soft, NT, ND
Peripheral pulses: 2+ DP
Musculoskeletal: pain in both arms, legs, and neck
Imaging:
CXR - clear and normal
Labs:
WBC 18.4
HGB 7.3
HCT 21.8
PLT 482
Na 138
K 4.7
Cl 108
CO2 26
BUN 6
Cr 0.6
Glucose 81
Ca 8.4
Retic 8.71
Retic Index 8.9
Assessment: 43 yo AAM with sickle cell crisis in arms, legs, neck, and head.
Problem List:
1. sickle cell crisis
2. increased white count
Differential Diagnosis:
He's presenting with acute onset of pain which is most likely related to a sickle cell crisis. He presents with no other signs, symptoms, or lab values suggesting other etiologies such as acute rheumatic fever, osteoid arthritis, or any other polyarticular arthritis. His pain is spread throughout his bones and joints which makes an SC crisis more likely.
His white blood count could be due to an infection, but he is not presenting with fever or any inflammatory reaction symptoms. He has no tachypnea, but he does have upper respiratory infection symptoms. His pulse ox is normal. His CXR is clear and this does not appear to be pneumonia. He should be worked up with urine cultures, urine analysis, and blood cultures.
Diagnostic Plan:
1. CBC w diff
2. Screen 8
3. Retic count and Retic Index
4. Blood Cx
5. Urine Cx
6. Urine Analysis
Therapeutic Plan:
1. Dilautid 4mg IV q4h
2. 125 cc/hr D5W
Causes of Chest Pain
Chest Pain |
Non-Cardiac |
Pulmonary |
|
Gastrointestinal |
|
Musculoskeletal |
Chostochondritis |
Other |
psychiatric |
Cardiac |
|
Tuesday, October 25, 2005
Internal Medicine
Wednesday, October 12, 2005
H and P for PDA
H and P
Patient Name:
Hospital Unit:
Time of Admission:
Informant:
Birthdate:
Age:
Sex:
CC:
Reason for Admission:
History of Present Illness:
Past Medical History:
Past Surgical History:
Injuries/Disabilities:
Medications:
Herbal Meds:
Immunizations:
Allergies:
Drugs:
Food:
Family History:
Social History:
Review of Systems:
General: ( ) weight loss ( ) fever ( ) night sweats ( ) weakness/fatigue ( ) appetite
Endocrine: ( ) heat intolerance ( ) decreased energy ( ) thyroid/reanl dz ( ) polydipsia ( ) polyuria
Lympatics: ( ) lymphadenopathy
Skin: ( ) itching ( ) pale ( ) palmar creases
Hematology: ( ) anemia ( ) bruising ( ) bleeding
Head: ( ) seizures ( ) trauma ( ) loss of conscioussness ( ) headache ( ) vertigo ( ) dizziness
Eyes: ( ) visual changes ( ) blurred vision ( ) loss of vision ( ) discharge
Ears: ( ) discharge ( ) ear pain ( ) tinnitus ( ) ototoxic drug history ( ) hearing loss
Nose: ( ) discharge ( ) rhinorrhea ( ) epistaxis
Mouth and Throat: ( ) lip cracking ( ) gum soreness ( ) gum hypertrophy ( ) dryness ( ) thirst ( ) excessive salivation ( ) throat pain ( ) hoarseness
Cardiorespiratory: ( ) SOB ( ) valvular disease ( ) orthopnea ( ) dyspnea on exertion ( ) nocturia ( ) edema ( ) paroxysmal nocturnal dyspnea ( ) cough ( ) cyanosis ( ) hemoptysis
Gastrointestinal ( ) dysphagia ( ) abdominal pain ( ) vomiting ( ) hematemesis ( ) melena ( ) hematochezia ( ) change in appetite ( ) diarrhea ( ) constipation ( ) jaundice
Genitourinary: ( ) change in bladder function ( ) change in amount ( ) dysuria ( ) hematuria ( ) discharge
Neuropsychiatric: ( ) weakness ( ) motor/sensory deficit ( ) depression ( ) anxiety
Pain:
Physical Exam
General Appearance:
Vital Signs:
Temperature: Oxygen Saturation: Blood Pressure:
Respiratory Rate: Pulse Rate:
Skin/Nails:
Head:
Eyes:
Ears:
Nose:
Throat/Mouth:
Neck:
Lymph:
Pulmonary:
CV:
Abdomen:
Breasts:
Rectal:
Genitals:
Peripheral pulses:
Musculoskeletal:
Neurologic:
Mental Status
CN I
CN II
CN III,IV, VI
CN V, VII
CN VII
CN VIII
CN IX, X
CN XI
CN XII
Cerebellar
DTRs
Labs:
Assessment:
Problem List:
Differential Diagnosis:
Diagnostic Plan:
Therapeutic Plan:
Sunday, October 09, 2005
Flash Drives Make Any Computer 'Personal'
Flash drives with built in software such as Migo allow users to carry their personal settings and files to any computer. Apparently, plugging in the USB flash drive will allow access to personal documents, e-mail, and internet favorites. It's a great idea for people who work in places with several computers and move among them, such as a hospital.
CMDT Review by MS3
Although CMDT appears as a tome of medicine at 1888 pages, its proven to be a good home reference book. Diseases are covered in a few pages, while still maintaining good attention to detail in presentation and management. This book is all text with a few tables and no pictures. More pages are dedicated to common diseases with varying presentations like pneumonia. It's main advantage over other books is it's updated every year. |
Washington Manual Handbook Review by an MS3
Saturday, October 08, 2005
Removing an Ink Stain from a Silk Tie
Wednesday, October 05, 2005
Tom Evans' ECG Cribsheets - PDA Version
This is a great guide to reading ECGs, and this can also be downloaded to a Palm PDA device. Download the zip file for Pocket PCs, and then install Pluckr for your Palm PDA and Sunrise Desktop for your computer. After extracting the zip file, send the index.html file to Sunrise, and then synch your Palm PDA.
Sunday, October 02, 2005
More than 100 Links for Medical Students
This page links to several free online resources. I especially like the anatomy links.
Saturday, October 01, 2005
Indications for Oxygen Therapy to Treat COPD
Source:
The Washington Manual of Medical Therapeutics, 31st edition.
Monday, September 26, 2005
Saturday, September 24, 2005
Practice questions for USMLE Step 2
Books for MS3 Surgery
Thursday, September 22, 2005
Free USMLE Step 1 and Step 2 practice questions
Sunday, September 18, 2005
Wednesday, September 07, 2005
Medical Student Surgery Hours
Start seeing patients 5 am
Round with the team 6 am
Operating Room 8 am to 4 pm
Evening Sign Out 6-7 pm
Sleep 9pm
Overnight Call every four days, Weekend call 24 hours starting at 6 am
Scrub Attire
Sunday, August 21, 2005
AccessMedicine on a PDA
Wednesday, July 27, 2005
Technology in Medicine
USMLE Score Reports
Thursday, July 21, 2005
Blueprints in Pediatrics
Saturday, July 16, 2005
Buying a PDA on eBay
Monday, July 11, 2005
Babies in Peds
Friday, July 08, 2005
First Full Day of Peds
Thursday, July 07, 2005
What I learned my first day of pediatrics
Sunday, July 03, 2005
Saturday, July 02, 2005
PDA for Rotations
Palm LifeDrive Its got a 4 gigabyte hard drive, which sets it apart from any other PDA on the market. Another distinguishing aspect is its price, $500. It might be more than I need for rotations at the hospital, but it would also serve as an mp3 player. | |
Treo 650 This PDA has everything bundled into one small package, including a a camera and a phone. I would only have to carry one device to the hospital, and its memory is expandable with SD cards. One drawback is its small size. The Treo has a much smaller screen than other PDAs after seeing it at an electronics store. The size is good for carrying it around as a phone, but I wouldn't be too happy staring at a small screen in the hospital. | |
Tungsten T5 The T5 is the top of the line flash drive based PDA, with a large 256 mb of internal memory. This is its main selling point, along with its fast processor and large screen. | |
Tungsten T3 The T3 is probably the best value for the money among the high end PDAs. Its got a large screen accessible by pulling open the PDA. Its a unique design, but I would rather have a large screen available at all times. | |
Tungsten E This is the minimum suggested PDA for rotations. Its got 32 mb of internal memory, which is enough for medical applications. |
Friday, July 01, 2005
Sunday, June 26, 2005
Saturday, June 25, 2005
Two Days Before Step 1
Wednesday, June 22, 2005
Monday, June 20, 2005
my life right now
Thursday, June 16, 2005
Sensitivity, Specificity, Positive Predictive Value, Negative Predictive Value
Go across for the PPV and NPV formulas; go down for the sensitivity and specificity formulas.
Actual | |||
+ | - | ||
+ | TP | FP | PPV |
- | FN | TN | NPV |
Sens | Spec |
Tuesday, June 14, 2005
Silicosis
Even ten to thirty years after exposure, silicosis can be asymptomatic. Patients can present with dyspnea, cough, or sputum production. Chest radiographs show small pulmonary nodules, from 1 mm to 10 mm, in the upper lobes of the lungs. Silicosis' complications include with lung cancer, chronic respiratory failure, and cor pulmonale. Patients should be treated for tuberculosis infections and other lung ailments. Other than for severe cases, prognosis is generally good for silicosis with possible mild respiratory symptoms.(2)
Medical Student Report
(1) Harrison's Online
(2) Hanley Pulmonology
McGraw-Hill's AccessMedicine
Monday, June 13, 2005
BRS Biochemistry
Sunday, June 12, 2005
BRS Behavioral Science
Wednesday, June 08, 2005
Higher Student Loan Interest Rates for 2005
BRS Pharmacology
Saturday, June 04, 2005
Reviewing Qbank
Levinson & Jawetz : Medical Microbiology & Immunology
Tuesday, May 31, 2005
Clinical Microbiology Made Ridiculously Simple
MedicalMnemonics.com | Browse | Browse by Category
Contains contributions from around the world. Also available for download onto a PDA.
Saturday, May 28, 2005
BRS Physiology
BRS Pathology
Tuesday, May 24, 2005
USF USMLE 1
http://www.med.usf.edu/2003/usmlesmack.html
Monday, May 23, 2005
The New York Times > Technology > Circuits > State of the Art: A New Spin on a Palmtop (or Inside It)
Great PDA, have to wait till the problems are worked out before it could be really useful in the field.
http://www.palmone.com/us/products/mobilemanagers/lifedrive/
High Yield Neuroanatomy
BRS Histology
Sunday, May 22, 2005
Gosling - Atlas of Human Anatomy
Saturday, May 21, 2005
Step 1 Released Questions
This is the software link for the 150 questions released by USMLE.org. It can be taken in a test format or untimed. Kaplan provides detailed explanations for this series of questions.
Friday, May 20, 2005
High Yield Anatomy
Wednesday, May 18, 2005
Student Loan Consolidation
Monday, May 09, 2005
Metabolic Bone Diseases
Condition | Thin Trabeculae | Numerous Osteoclasts | Excessive Osteoid | Fibroblast/ Collagen |
Osteoporosis | X | |||
Osteomalacia | X | |||
Primary Hyperparathyroidism | X | X | ||
Renal Osteodystrophy | X | X | X |
Sunday, May 08, 2005
Dermatopathology II
Disease | Pathogenesis | Pathology | Clinical Features/ Treatment |
Erythema nodosum | trigger: drugs, microorganisms, systemic diseases drugs: sulfonamides | fibrous septa of subcutaneous tissue - neutrophil inflammation, extravasation of erythrocytes | dome-shaped, tender, nodules on extensor surface of legs 3rd decade, 3xF:M |
Erythema induratum | Mycobacterium tuberculosis | initially lobular panniculitis, vasculitis - ischemic necrosis of fat lobules | chronic, recurrent, subcutaneous plaques or nodules on legs, women T - systemic steroids |
Scleroderma | pathcy lymphocytic infiltrate, loss of peri-eccrine fat, plugging of sweat glands, obliteration of hair follicles, subcutaneous fat turns into collagen | fibrosis and tightening of skin | |
Granulomatous dermatitis | localized collection of epitheliod macrophages around insoluble antigen | ||
Allergic Contact dermatitis | sensitization - haptens: oleoresins, Langerhans Cells - CD4+ T cells | spongiotic dermatitis - edema in epidermis spongiotic vasculitis - vacuoles filled with lymphocytes and macrophages | immune rxn to poison ivy, poison oak, poison sumac |
Source: Rubin's Pathology 4th Edition
Dermatopathology I
Disease | Pathogenesis | Pathology | Clinical Features/ Treatment |
Pemphigus Vulgaris | antibodies to keratinocytes, autoimmune IgG to desmoglein 3 | seperation of stratum spinosum and outer epidermal layers from basal layer | blistering skin large, scalp, mucous membranes, periumbilical and intertriginous areas |
Diseases of the Basement Membrane Zone | |||
Epidermolysis Bullosa | hereditary | splitting of epidermis at or near basement membrane | blisters |
Epidermolytic EB | disruption of basal keratinocytes | vacuoles filled with abnormal keratin 5 and 14 | blisters from minor trauma - no scarring |
Junctional EB | AR | lamina lucida blister | blisters |
Dermolytic EB | defect in anchoring fibrils, defective collagen type VII | roof - normal epidermis, lamina lucida, lamina densa | atrophic scarring |
Bullous Pemphigoid | complement fixing IgG antibodies to BPAG1 and BPAG2 | subepidermal blisters roof - intact epidermis base - lamina densa cytology - numerous eosinophils, arranged along BMZ seperation at lamina lucida | large, tense blisters T - corticosteroids |
Source: Rubin's Pathology 4th Edition
Saturday, May 07, 2005
Psoriasis
Disease | Psoriasis |
Pathogenesis | Genetic factors - HLA-B13,HLA-B17, HLA-Bw57, HLA-Cw6 increased Environmental factors - physical injury, infection, drugs Abnormal cellular proliferation of keratinocytes microcirculatory changes - "bridged" fenestrations, neutrophils at tipsof dermal papillae, dec cAMP Immunologic factors - T cell infiltration |
Pathology | thickened epidermis -hyperkeratosis + parakeratosis uniformally elongated rete ridges and dermal papillae dilated and tortuous capillaries of papillae epidermal hyperplasia Munro microabscesses - dense collection of neutrophils |
ClinicalFeatures/Treatment | large, erythematous, scalyplaques dorsal extensor cutaneous surfaces 7% - seronegative arthritis, mild neutrophilic pustules T - coal tar or wood tar, anthralin, corticosteroids, methotrexate,vitamin A, vitamin D |
Ichthyosis
Disease | Pathogenesis | Pathology | ClinicalFeatures/Treatment |
Ichthyoses | increasesed cohesiveness,abnormal keratinization, increased basal cell proliferation | abnormally thickened stratumcornerum, hyperkeratosis, thin nucleated epidermis | coarse, fish-like scales |
Ichthyosis Vulgaris | Autosomal Dominant - reduced or absent keratohyaline granules in epidermis attenuated stratum granulosum - reduced profilaggrin | loose stratum corneum,basket-weave appearance | most common, begins earlychildhood, small white scales on extensor surfaces of extremities andon trunk and face, lifelong disease abnormalities in lipid metabolism from drugs or other diseases |
X- linked ichthyosis | deficiency of sterioid sulfatase steroid sulfatase degrades cholesterol sulfate | persistent cohesion of stratumcorneum | |
Lamellar ichthyosis | autosomal recessive - disorderof cornification, defect in lamellar body secretion | increased cohesivenss of stratumcorneum, numerous keratinosomes, abnormally large amount ofintercellular substance | severe and generalized ichthyosis |
Epidermolytic hyperkeratosis | autosomal dominant, mutation inkeratin genes in suprabasal epidermis | faulty assembly of keratintonofilaments, impaired insertion into desmosomes, prevents normaldevelopment of cytoskeleton -> epidermal lysis and vesicles | generalized erythroderma,blistering, ichthyosiform skin |
Skin Layers and Diseases
Layer of Skin | Associated Disease |
Basement Membrane | Bullous pemphigoid - antibodies to BPAG1 and BPAG2 - Type XVII colagen |
Papillary dermis | psoriasis, lichen planus |
Recticular dermis | scleroderma, erythema nodosum |
Source: Rubin's Pathology 4th Edition
Skin Cell Types
Cell Type | Function | Structures |
Melanocytes | color of the skin | melanosome - melaninsynthesis |
Langerhan cells | antigen presenting cells | Birbeck granules, MHC I, MHC II,receptors for Fc IgG and Fc IgE |
Merkel Cell | neurosecretory, tactilemechanoreceptor | form desmosomes with keratinocytes, basal aspect apposed to a small nerve plate |
Keratinocytes | produce keratin filaments | Keratohyaline granules, Odlandbodies - keratinosomes |
Source: Rubin's Pathology 4th Edition
Gynecological Pathology Endometrium
Condition | Cause | Pathology/Histology | Clinical Features | Other Features |
Proliferative Enodmetrium | · Straight glands · Narrow lumens · Pallisading nuclei · Ovoid nuclei · Mitoses | |||
Early Secretory Endometrium | First manifestation of effect of ovulation on endometrium | · Glands remain straight · Lumens remain narrow · Subnuclear vacuoles appear | 24-36 hours after ovulation | |
Mid Secretory Endometrium | · Glands become coiled · Vacuoles no longer present in glands · Secretory product appears in lumen | Postovulatory days 5-9 | ||
Late Secretory Endometrium | · Intralumenal secretions are spent · Stromal predecidua appears · First predecidua around spiral arteries · Later predecidua beneath surface | Postovulatory days 10-14 | ||
Menstrual Endometrium | · Stromal collapse · Fribrin thrombi and blood · Glands are broken apart · Glands have no secretions | |||
Hyper-secretory Endometrium of Pregnancy | · Arias-Stella reaction · large, hyperchromatic nuclei · prominent cytoplasmic vacuolization | |||
Atrophic endometrium | · short glands · glandular cells – flat, without significant mitotic activity | |||
Dysfunctional Uterine Bleeding | · anovulatory bleeding · luteal phase defect | |||
Unopposed Estrogen | · proliferative glands · stromal breakdown · fibrin thrombi · wreathing of stroma by glandular cells | |||
Contraceptives | Combined oral agents | · mix of proliferative and secretory changes · long use · atrophic glands · stromal predecidual pattern dominates | ||
Depoprovera | · unopposed progesterone | |||
Tamoxifen | · inc risk of carcinoma · inc incidence of polyps · large, mucinous metaplasia, fibrotic | |||
Endometrial Hyperplasia | · unopposed estrogen stimulation – exogenous, endogenous · no progestational stimulation | · simple or complex architecture · typical or atypical nuclei | Vaginal bleeding, 60s Risk factors – obesity, diabetes, nulliparity, early menarche, late menopause | Complex atypical hyperplasia progresses to carcinoma – 1/3 T – hysterectomy, hormonal manipulation |
Endometrial Carcinoma Type 1 Endometrioid | · PTEN gene mutation à cell growth and apoptosis | · squamous or mucinous | Grade determines prognosis T – hysterectomy, good survival Low grade – hormonal | |
Endometrial Carcinoma Type 2 Unfavorable Histology | · serous-p53 mutations | · clear cell | Early spread outside uterus long term survival uncertain |
Gynecological Pathology I
Condition | Cause | Pathology/Histology | Surface Features | Other Features |
Vulvar Malgnancies | ||||
Vulvar Intraepithelial Neoplasia | HPV | Varying degrees of loss of maturation of squamous cells | Single or multiple plaques or papules | Co-exists with cervical dysplasia |
Invasive squamous cell carcinoma | Keratinizing squamous cell histology | Ulcerated exophytic lesions | Most common vulvar malignancy | |
Verrucous carcinoma | Well differentiated, locally invasive | Giant condyloma | Unlikely to metastasize, subset of invasive squamous cell carcinoma | |
Extramammary Paget’s Disease | Intraepithelial adenocarcinoma in the vulva | Red, moist plaque | ||
Malignant Melanoma | Same as skin melanoma | Second most common malignant tumor in vulva | ||
Benign Disorders of Vulva | ||||
Lichen Sclerosis | Atrophic epidermis, hyalinized epidermis | White plaques | ||
Squamous hyperplasia | Thickened epidermis | White plaques | ||
Hidradenoma | Benign tumor | Sweat gland origin – apocrine | ||
Syringoma | Benign tumor | Sweat gland origin – eccrine | ||
Hemangioma | Benign tumor | Mesenchymal | ||
Vagina | ||||
Failure of squamous cell maturation | Absence of estrogen | |||
Adenosis | DES exposure, sporadic | Abnormal retention of embryologic glandular epithelium | ||
Benign disorder | ||||
Squamous cell carcinoma | Vaginala intraepithelial neoplasia | Most common vaginal neoplasm, assoc w cervical and vulvar SSC, 80% spread from cervix | ||
Clear Cell Adenocarcinoma | Prior DES exposure | Peak age 17-22, very uncommon | ||
Embryonal Rhabdomyosarcoma | Sarcoma of primitive skeletal muscle | Sarcoma botryoides – grape like | Seen in young children | |
Cervix | ||||
Cervical Intraepithelial Neoplasia | HPV esp types 16,18, 31, 33, 35 Ã Inactivation of suppressor gene products p53 and Rb | Occurs in transition zone Degree of loss of maturation in squamous cells | ||
Invasive Carcinoma of Cervix | Microinvasion, non-keratinizing squamous cel,l Advancing disease can obstruct ureters, invade locally | Adenocarcinoma – less common, more aggressive 2nd most common cause of death WW |
Gynecological Pathology
Condition | Cause | Pathology/Histology | Clinical Features | Other Features |
Proliferative Enodmetrium | · · · · · | |||
Early Secretory Endometrium | First manifestation of effect | · · · | 24-36 hours after ovulation | |
Mid Secretory Endometrium | · · · | Postovulatory days 5-9 | ||
Late Secretory Endometrium | · · · · | Postovulatory days 10-14 | ||
Menstrual Endometrium | · · · · | |||
Hyper-secretory Endometrium | · · | |||
Atrophic endometrium | · · | |||
Dysfunctional Uterine Bleeding | · · | |||
Unopposed Estrogen | · · · · | |||
Contraceptives | Combined oral agents | · · · · | ||
Depoprovera | · | |||
Tamoxifen | · · · | |||
Endometrial Hyperplasia | · · | · · | Vaginal bleeding, 60s Risk factors – obesity, diabetes, nulliparity, early menarche, late | Complex atypical hyperplasia T – hysterectomy, hormonal manipulation |
Endometrial Carcinoma Type 1 | · | · | Grade determines prognosis T – hysterectomy, good survival Low grade – hormonal | |
Endometrial Carcinoma Type 2 | · | · | Early spread outside uterus | |
Uterine Mesenchymal Tumors | ||||
Leiomyoma | · | · · · · | Extremely uncommon | |
Leiomyosarcoma | · | · · · | ||
Stromal Sarcoma | · | · · | Appearance of endometrial stroma | T- hormonal therapy |
Uterine Mixed Tumors | ||||
Adenomyoma | · | · | ||
Adenosarcoma | · | · | ||
Carcinosarcoma | · | · | ||
Fallopian Tube | ||||
Infection | · · | Important cause of infertility | ||
Ecotpic Pregnancy | · | Ruptured fallopian tube is life | Most common site of ectopic | |
Ovary and Placenta | ||||
Polycystic Ovary Syndrome (Stein-Levanthal) | - - | - - | ||
Endometriosis | - - - - | - | - - | |
Ovarian Tumors | - | - | - | |
Ovarian Epithelial Carcinomas | - - - - - | - | - | Highest mortality rate of female Difficult to detect early, spread beyond ovaries Adults, first-degree relatives, industrialized Inc with age, dec with parity and oral contraceptive |
Benign Ovarian Germ Cell Tumors | - | - - - - | - | Wide age range |
Malignant Ovarian Germ Cell | - | - - - - | - | Highly malignant course but Exclusively children, young adults |
Sex Cord Stromal Tumors | - | - | - | - - |
fibroma | - | - | - | - |
Thecoma | - | - | - | - |
Granulosa cell tumor | - | - | - | - |
Sertoli-Leydig cell tumor | - | - | - | - |
Metastatic Tumors to the Ovary | - | - | - | - - |
Placenta | - | - | - | - |
Chorioamnionitis | - - | - | - | - - |
Villitis | - - | - | - | - |
Sponataneous Abortion | - - - - - | - | - | - - |
Septic Abortion | - | - | - | - |
Toxemia of Pregnancy | - - - | - | - - - - | - |
Placental Abnormalities | - | - | - | - |
Retroplacental Hematoma/ Abruption | - - | - | - | - |
Placenta Accreta | - | - - | - | - |
Gestational Trophoblastic | - | - | - | - |
Complete Hydatidiform Mole | - - - | - | - | - |
Partial Hydatidiform Mole | - - | - | - | - |
Choriocarcinoma | - | - | - - | - |