48 PANCE Medical Syndrome Questions 150605 Flashcards

(48 cards)

0
Q

This patient presents with mouth sores, skin rashes, uveitis, arthralgia, small vessel vasculitis, and confusion leading you to a diganosis of ____.

A

Behcet’s Syndrome

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1
Q

A patient presents with irregular periods, pain during menstruation, repeated miscarriage, infertility and endometrial adhesions leading you to a diagnosis of ____.

A

Asherman’s Syndrome

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2
Q

A patient presents with loss of pain and temperature sensation on contralateral side of body and loss of proprioception and discriminatory touch on the ipsilateral side of the body leading you to a diagnosis of ____.

A

Brown-sequard Syndrome

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3
Q

A patient presents with burning sensation in the chest, food regurgitation, weight loss and a history of GERD leading you to suspect ____.

A

Barret’s Syndrome (Esophagus)

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4
Q

A patient presents with Mackler’s triad and excruciating retrosternal chest pain after an episode of straining leading you to suspect ____.

A

Boerhaaves Syndrome

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5
Q

A patient presents with a classic triad of abdominal pain, ascites, and hepatomegaly and evidence of hepatic vein thrombosis leads you to suspect ____.

A

Bud-chiari Syndrome

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6
Q

A patient presents with diarrhea, flushing, ascites, and bronchospasm with elevated urine 5HIAA, elevated serum Serotonin and Kallikrein leading you to suspect ____.

A

Carcinoid Syndrome

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7
Q

A patient presents numbness and tingling in the first three and a half digits with a history of hypothyroidism leading you to suspect _____.

A

Carpal Tunnel Syndrome

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8
Q

This syndrome also goes by the name of eosinophilic granulomatosis with polyangiitis which occurs in three stages, allergic stage, eosinophilic stage and vasculitic stage suggesting ____.

A

Churg-strauss Syndrome

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9
Q

An inherited disorder affecting the conjugation of bilirubin that lethargy, jaundice and confusion. Biopsy and serum bilirubin testing may suggest ____.

A

Crigler-Najjar Syndrome

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10
Q

A patient presents with abdominal obesity, thinning skin, poor wound healing, proximal muscle weakness, hypertension, buffalo hump, moon facies and elevated serum cortisol levels suggest a diagnosis of ____.

A

Cushing’s Syndrome

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11
Q

Deletion of a portion of the 22nd chromsome resulting in cleft palette, tetrology of Fallot and failure to thrive should make you think of ____.

A

Digeorge Syndrome

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12
Q

A genetic mutation that causes short ears, hypotonia, large tongue, epicanthal folds, mental retardation and a Karyotype that reveals trisomy 21 suggests a diagnosis of ____.

A

Down Syndrome

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13
Q

An asymptomatic syndrome that is autosomal recessive and causes elevation serum bilirubin without elevation of LFTs suggests ____.

A

Dubin-johnson Syndrome

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14
Q

Patient is born with a small, abnormally shaped head, MR and a karyotype that has trisomy 18 suggests ____.

A

Edward’s Syndrome

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15
Q

Connective tissue disorder and a patient presenting with stretchy skin, hx of osteoarthritis, and valvular heart disease suggests a diagnosis of ____.

A

Ehlers-danlos Syndrome

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16
Q

Symptoms of polyuria, polydipsia, dehydration and growth retardation due to proximal renal tubule disease that inhibits reabsorption of glucose, amino acids, uric acid, phosphate and bicarbonate suggests ____.

A

Fanconi Syndrome

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17
Q

A patient presents with symptoms of arthralgias, morning stiffness, splenomegaly and neutropenia suggesting a diagnosis of ____.

A

Felty’s Syndrome

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18
Q

A patient presents with abdominal pain aggravated by breathing that radiates to the right shoulder with a history of pelvic inflammatory disease suggesting a diagnosis of ____.

A

Fitz-hugh-curtis Syndrome

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19
Q

An infant arrives at the clinic that demonstrates below average height/weight, low birth weight, developmental delay, smooth philtrum, and congenital heart defects suggesting a diagnosis of ____.

A

Fetal Alcohol Syndrome

20
Q

A peripheral nervous system disorder that starts with weakness at the extremities spreading towards the trunk suggests a diagnosis of ____.

A

Guillain-barre Syndrome

21
Q

Also known as anti-glomerular basement antibody disease, a patient may present with hematuria, hemoptysis, and shortness of breath due to lung and kidney injury leading you to a diagnosis of ____.

A

Goodpasture’s Syndrome

22
Q

Miosis, Ptosis, anhirdosis, on the same side as the lesion suggests a diagnosis of ____.

A

Horner’s Syndrome

23
Q

A patient comes in with chronic or recurrent abdominal discomfort along with either predominantly diarrhea or constipation leading you towards a diagnosis of ____.

A

Irritable Bowel Syndrome

24
A patient presents with chronic upper and lower respiratory tract infections in conjunction with sinus congestion, otorrhea and sterility in males suggesting a diagnosis of _____.
Kartagner's Syndrome
25
A patient presents with hypogonadism, sterility, low energy, lean body, developed breat tissue, with a karyotype of 47, XXY suggesting a diagnosis of ____.
Klinefelter's Syndrome
26
This patient presents with short term memory loss and difficulty learning new information with a tendency to confabulate leading you to draw a thiamine level which is decreased suggesting a diagnosis of ____.
Korsakoff Syndrome
27
This patient presents with proximal muscle weakness that makes climbing stairs and rising from sitting extremely difficult. The patient does report that stength improves with repeated testing.
Lambert-eaton Syndrome
28
Patient reports palpitations, lightheadedness and SOB with an EKG suggesting atrioventricular re-entrant tachycardia suggesting a diagnosis of ____.
Lown-ganong-levine syndrome
29
A patient presents with a medical history that seems inconsistent and dramatic and you suspect that they are here for second gain leading you to a diagnosis of _____.
Munchausen Syndrome
30
A tall skinny basketball player has incidental findings of heart valve defects and aortic aneurism suggesting a diagnosis of ____.
Marfan Syndrome
31
A patient with a history of lung cancer comes to you with severe sholder pain radiating to the axilla with upper extremity atrophy and horner's syndrome suggesting a diagnosis of ____.
Pancoast Syndrome
32
A young patient has a history of multiple polyps of the stomach and intestines during childhood with a high risk of developing cancers of GI tract, pancreas, cervix, ovary and breast leading you to the diagnosis of ____.
Peutz-jeghers Syndrome
33
This child presents with a several day history of rash, hyperventilation, and confusion several days after having been given aspirin during a viral illness leading you to a diagnosis of ____.
Reye's Syndrome
34
This patient comes in with several month history of joint pain, red eyes and painful urination leading you to a diagnosis of ____.
Reiter's Syndrome
35
A patient comes in with irresistable sensations of having to move her legs while reading or trying to sleep suggesting a diagnosis of ____.
Restless Leg Syndrome
36
A young infant presents to the hospital with lesions of bullous impetigo, erythema and redness over most the body and you suspect a complication of staphylococcal infection known as ____.
Scalded Skin Syndrome
37
A patient comes into the clinic complaining of dry eyes, dry mouth, dry skin and joint pain prompting you to add ____ to your differential.
Sjogren's Syndrome
38
A female comes in with irregular periods, hirsutism, acne, dark skin markings and male pattern baldness swaying you towards a diagnosis of ____.
Stein-levanthal syndrome, Polycystic Ovarian Syndrome
39
A patient with a history of depression comes in agitated, confused, tachycardic, shivering and with dilated pupils suggesting a diagnosis of ____.
Serotonin Syndrome
40
A patient comes in with symptoms of lightheadedness, fatigue, shortness of breath and repeated episodes of unexplained syncope leading you to a diagnosis of _____.
Sick sinus syndrome
41
This patient presents with swelling of the face and tongue with a blistering red rash and painful shedding of skin. He reports recent medication changes leading you to worry about a life-threatening diagnosis of _____.
Steven-Johnson Syndrome
42
A patient with a history of lung cancer, tuberculosis and syphilis presents with SOB, HA, JVD, and facial and upper extremity edema making you suspicious for ____.
Superior Vena Cava Syndrome
43
This patient presents with fatigue, chest pain, shortness of breath, extremity weakness/pain, joint pain and syncope. MRA reveals a large vessel vasculitis leading you to conclude the patient has ____.
Takayasu's Syndrome
44
I say fever, hypotension, elevated white count and tampon, then you say ____.
Toxic Shock Syndrome
45
This female patient comes in with a short webbed neck, short stature, obesity, broad chest and widely spaced nipples along with infertility and amenorrhea. You are not surprised that karyotyping reveals 45X, a missing X chromsome. You are absolutely convinced she has ____.
Turner Syndrome
46
This dude comes into the hospital with palpitations and dizziness. EKG reveals an SVT of the atrioventricular reciprocating type along with some fairly diagnostic delta waves. You impress the on call cardiologist by correctly diagnosing ____.
Wolff-Parkinson White Syndrome
47
This patient arrives in your clinic with a long history of peptic ulcer disease and reflux. You correctly order ____ to confirm your diagnosis of ____.
Gastrin, Zollinger-Ellison Syndrome