Random Flashcards

1
Q

Most common nail finding in PsA

A

Nail pitting

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2
Q

Most common PsA phenotypes

A

Oligoarthritis (>70%)
Polyarthritis (15%)

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3
Q

Most common sites of enthesitis (found in PsA)

A

Achilles tendon
Plantar fascia
Lateral epicondyles at elbows

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4
Q

Strongest genetic risk for PsA in patients with psoriasis vulgaris

A

HLA-B27

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5
Q

These tests are recommended to differentiate PsA from rheumatoid arthritis

A

Rheumatoid factor
Anti-CCP

(negative results will favor RA)

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6
Q

For PsA, how many months to maximize chances of minimal disease damage

A

6 months

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7
Q

This DMARD is preferred for peripheral spondylitis and improves psoriatic joint swelling. (NO SKIN improvement)

Reversible azoospermia may be seen

A

Sulfasalazine

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8
Q

This selective PDE4 inhibitor has moderate effects on PsA for skin, nails, joints, but may cause depression

A

Apremilast

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9
Q

These TNF inhibitors are effective for PsA with UVEITIS and IBD

A

Infliximab
Adalimumab

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10
Q

An inhibitor of common p40 subunit of IL12 and IL23, approved for Psoriasis and PsA, effective if with IBD and Crohn’s

A

Ustekinumab

But can cause eosinophilic pneumonia and cancer

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11
Q

This TNF-inhibitor can cause drug-induced SLE

A

Etanercept

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12
Q

Patient presents with urethral, ocular, and articular inflammation is seen in what disease

A

Reactive arthritis
(aka Reiter syndrome)

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13
Q

Patient presents with bloody diarrhea, dysuria with purulent discharge, conjunctivitis and photophobia, what is the diagnosis? Expected lab findings?

A

Reactive arthritis

Non-specific increased ESR, CRP, platelet count
Synovial fluid is sterile
Gram stain is negative

Can culture the urethra for Chlamydia

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13
Q

Criteria for diagnosing Reactive Arthritis

(in my own words)

A
  1. Arthritis should involve lower limb and should be asymmetric
  2. Should have history of bloody diarrhea or UTI at least 4 weeks prior
  3. No joint infection
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14
Q

This presents as erythematous vesicular-pustular keratotic lesions on the palms and soles coalescing into psoriatic-like plaques

A

Keratoderma blenorrhagicum

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15
Q

This presents as an erythematous papule or pustule with raised borders around the penile meatus, shaft, or glans.

If circumcised, becomes a hard, dry crust resembling a psoriatic plaque

A

Circinate balanitis

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16
Q

Etiology and pathogenesis of Rheumatic Fever

A

Pharyngitis caused by Grp A beta-hemolytic streptococcal infections triggers an abnormal inflammatory immune response. This cross-reacts with the myocardium, synovium, and basal ganglia chorea.

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17
Q

What is the common valve affected in rheumatic fever?

A
  1. Mitral Valve
  2. Aortic Valve
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18
Q

Patient presents with annular evanescent, erythematous patches along the torso, upper arms, legs

A

Think of erythema marginatium

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19
Q

Major Criteria for Acute Rheumatic Fever

A
  • Carditis
  • Chorea (jerky movements)
  • Erythema marginatum
  • Subcutaneous nodules
  • Arthritis
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20
Q

This drug can cause ARF-like syndrome called erythema marginatum hemorrhagicum

A

Sorafenib

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21
Q

Treatment for Acute Rheumatic Fever

A

Penicillin VK
- 250mg BID for children
- 500mg BID for adults

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22
Q

Acute rheumatic fever occurs when?

A

2-3 weeks after a throat infection, more common in ages 5-15 years old

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23
Q

Patient with a history of URTI presents with nonpitting neck induration that appear waxy and smooth, with prominent follicular ostia giving a peau d’orange appearance.

Diagnosis and treatment options

A

Scleredema
Associated with diabetes

Treat the DM, UVA1 may be helpful

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24
Q

Major fibroblast products in scleredema-affected skin

A

Type 1 collagen and hyaluronate

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25
Q

Adult patient presents with generalized lichenoid eruption of minute papules on the extremities and trunk with bovine facies

Diagnosis and associated pathogenesis

A

Scleromyxedema

Monoclonal paraproteinemia of Immunoglobulin G-kappa

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26
Q

10/male presented with fever for the past 2 weeks, 39C twice a day - accompanied by evanescent, erythematous, salmon pink macular rash. Lymphadenopathy is present.

A

think Juvenile Idiopathic Arthritis

27
Q

Macrophage Activation Syndrome (MAH)

potentially life-threatening complication of rheumatic disorders

A

febrile patient with known or suspected sJIA who has a ferritin value >684 ng/mL and also exhibits any 2 of the following:
- platelet count ≤181
- aspartate aminotransferase >48 units/L
- triglycerides >156 mg/dL
- fibrinogen ≤360 mg/dL

28
Q

Macrophage Activation Syndrome (MAH)

A
  • associated with thrombotic thrombocytopenic purpura
  • hemorrhage
  • irritability, seizure, coma
29
Q

Two serious complications of Adult-Onset Still Disease

A
  • reactive hemophagocytic syndrome
  • thrombotic thrombocytopenic purpura
30
Q

D-penicillamine therapy can cause what acquired perforating disorder?

A

Acquired elastosis perforans serpiginosa

31
Q

Most common cardiac defect in Marfan Syndrome

A

Medial necrosis of the aorta

32
Q

Most common cardiac defect in Marfan Syndrome

A

Medial necrosis of the aorta

33
Q

Death in Marfan patient occurs due to?

A

Aortic dissection rupture and pericardial tamponade

34
Q

A patient is noticeably tall, thin, and with striae on the upper chest, arms, thighs, and abdomen.

What is the gene defect and diagnosis?

A

FBN1 gene (fibrillin 1)
Marfan Syndrome

35
Q

A tall and thin patient with ectopa lentis came in for consult for derma clearance. What ophthalmic procedure is contraindicated?

A

LASIK
(Marfan Syndrome patient, FBN1 gene)

36
Q

A female patient came in with yellowish, flat-topped, discrete, confluent papules on the neck and flexural areas.

What eye findings are most common?

A

Eye findings: Angioid streaks, radial curvilinear extensions of gray, brown, red discolorations
Diagnosis: Pseudoxanthoma elasticum

37
Q

A female patient with yellowish papules in a pebbly pattern on the flexural areas came in for biopsy.

What biopsy findings do you expect? Stains?

A

Histopath: Broken curls of basophilic elastic fibers - swollen, tortuous, and irregularly clumped

Stains:
Elastic fibers - Verhoeff von Gieson
Calcium - von Kossa

38
Q

A 25/F with symmetric, tender, erythematous nodules on the anterior legs and ankles came in for consult. She has history of URTI one week prior.

What is your diagnosis and treatment?

A

Diagnosis: Erythema Nodosum
Treatment:
- treat underlying infection
- after which…
- give NSAIDs
- SSKI 2-10 drops 3x/day
- Colchicine
- Etanercept, Infliximab

39
Q

A 35/F with symmetric, tender, erythematous nodules on the anterior legs and ankles came in for consult. You do not see any ulceration. Biopsy was done. What are the histopath findings?

A

Erythema Nodosum, wherein you will see septal panniculitis and the characteristic Miescher granuloma (histiocytes surrounding a central stellate cleft)

40
Q

Histopath findings on a leg biopsy showed septal panniculitis with Meischer granuloma. What are the most common etiologic agents associated with the disease?

A

Erythema Nodosum
Causes - underlying infection
In Pedia - Strep throat infection
Recurrent - sarcoidosis, hormonal therapy, pregnancy, strep infection

41
Q

A 35/F came in for consult with recurrent erythematous nodules with ulceration on the posterior calf.

What should you investigate for and histopath findings?

A

Case of Erythema Induratum

Investigate for MTB
Histopath will show lobular panniculitis and extensive necrosis of adipocytes in the center of adipose

42
Q

Potential markers for extrapancreatic fat necrosis

A

Resistin and Leptin

43
Q

Potential markers for extrapancreatic fat necrosis

A

Resistin and Leptin

44
Q

These drugs can cause HAART-induced lipodystrophy in HIV patients

A

Nucleoside analogs - Zidovudine and Stavudine
They induce fat loss by inhibiting polymerase-y

45
Q

An 8/F came in with hypopigmented skin. You noticed her hair was silvery. What is diagnostic for this and what is the diagnosis?

A

Check the hair for large clumps of pigment in the hair shaft.
Griscelli Syndrome

46
Q

Patient presents with segmental vitiligo on the face, with poliosis, ipsilateral hearing loss, and visual changes.

Diagnosis?

A

Alezzandrini syndrome

47
Q

Patient presents with segmental vitiligo on the face, with poliosis, ipsilateral hearing loss, and visual changes.

Diagnosis?

A

Alezzandrini syndrome

48
Q

Patient presents with hearing loss, visual changed, meningitis, and flu-like symptoms. Depigmentation and poliosis presented after the systemic symptoms. Diagnosis?

A

Vogt-Koyanagi-Harada syndrome

49
Q

Mucocutaneous pigmentation and intestinal hamartomas are the hallmarks of this condition

A

Peutz-Jeghers Syndrome (STK11)
commonly associated with GI malignancy

50
Q

Most sensitive test for PCOS

A

Free Testosterone

51
Q

The only FDA-approved OTC treatment for acne 12 yrs old and older

A

Adapalene 0.1% Gel

52
Q

What does Verhoeff van gieson stain detects?

A

Elastic fibers

53
Q

What does von kossa stain detects in PXE?

A

Calcium deposition in elastic fibers

54
Q

Most frequent clinical pattern of AGA in men

A

Recession of frontal hairline in a triangular pattern

55
Q

Most common type of AGA pattern in women

A

Diffuse thinning of centroparietal region with maintenance of frontal hairline

56
Q

Adrenal adenomas secrete:

A

Testosterone

57
Q

Adrenal carcinomas secrete:

A

Testosterone, DHEAS, and cortisol

58
Q

The only drug approved for the removal of facial hair:

A

Topical eflornithine
- inhibits ornithine decarboxylase, which shortens the hair growth cycle

59
Q

The only drug approved for the removal of facial hair:

A

Topical eflornithine
- inhibits ornithine decarboxylase, which shortens the hair growth cycle

60
Q

Popping or snapping to augment sexual pleasure uses these inhalants:

A

Amyl nitrite or butyl nitrite

61
Q

Popping or snapping to augment sexual pleasure uses these inhalants:

A

Amyl nitrite or butyl nitrite

62
Q

Cold urticaria with deafness and amyloidosis may be associated with this syndrome

A

Muckle-Wells syndrome
causative agent: probably H. pylori

64
Q

Prednisone dose sufficient to withhold live-virus vaccine (measles, oral polio, vaccine)

A

more than or equal to 2mg/kg/day or 20mg/day for children weighing more than 10kg, given more than 14 days

65
Q

Recurrent crops of follicular papules and pustules that form an annular pattern on the face and arms in a Japanese patient

A

Ofuji Disease

66
Q

Elderly male with pruritic red-to-brown confluent papules with a cobblestone appearance, sparing the abdominal folds

A

Papuloerythrodrrma of Ofuji
(+) deck-chair sign
(+) peripheral blood eos