Interstitial Lung Disease CIS Flashcards

1
Q

75 year old male with an abnormal chest x-ray. He had a normal chest x-ray six months ago. He has a 60 pack year smoking history. Three weeks ago he noticed myalgias in his shoulder and neck along with fatigue and a sinus infection. He was treated with antibiotics 2 weeks ago by another doctor with no results. In the past four days he has had hemoptysis with blood streaked sputum. He has had a 20 lb weight loss for the past month. Exam reveals a temperature of 99F. Scattered crackles are heard bilaterally. There are no skin findings and no joint findings. Your office chest x-ray shows bilateral lung nodules, some of which have cavitated

Hgb 9.2g/dL
WBC 10,700
Na  131
K 5.2
CA 8.0mg/dl
Creatinine 6 mg/dl
UA 51-100 rbc/hpf, 4-10 WBC/hpf

The most likely diagnosis is:

A.  Acute interstitial fibrosis
B.  Disseminated histoplasmosis
C.  Wegner’s granulomatosis
D.  Metastatic bronchoalveolar cell carcinoma
E.  Goodpasture’s syndrome
A

wgeners granulomatosis

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2
Q

Differential Diagnosis of Cavitary Lung Lesions

A

C Carcinoma: squamous cell, melanoma, cervical, sarcoma metastasis
A Autoimmune: Wegner’s, rheumatoid lung
V Vascular: bland/septic emboli
I Infection: TB, fungal (coccidio, aspergillosis, cryptosporidia, nocardia) bacterial ( esp. GNR, staph, strep
T Trauma
Y Young congenital lesions (bronchogenic cyst or communicating sequestration

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3
Q

61 year old male has worsening shortness of breath over the last year. He now becomes short of breath walking only a short distance, and has trouble with simple activities of daily living. This resolves when he lies down. He has a hacking cough that is nonproductive. He admits to a 50 pack year history of smoking, though he quit 5 years ago. Past medical history is significant for atrial fibrillation, hypertension, rheumatoid arthritis, and depression. Current medications include amiodarone, hydrochlorothiazide, and methotrexate.

BP 135/85 mm Hg, P 83/min, RR 25/min, and Temp 98.6 F Chest examination reveals diffuse, dry, “Velcro-like” crackles two thirds of the way up the chest. Cardiac examination shows an elevated jugular venous pressure and a widely split S2. The extremities have 1+ pitting lower extremity edema and marked clubbing. A chest radiograph shows mild bibasilar interstitial reticular markings and some possible atelectasis.

PFT’s show:
FVC 2.31 L 52% of predicted
FEV1 1.89 L 51% of predicted
FEV1/FVC 0.81 98% of predicted

Which of the following is the most appropriate next step in management?
A. Perform a methacholine challenge test.
B. Empiric trial of interferon and steroids
C. Start him on high dose oral corticosteroids
D. Stop amiodarone and methotrexate, follow pulmonary function tests
E. Initiate bronchodilator therapy with albuterol and add an inhaled steroid

A

stop amiodarone and methotrexate, follow pulmonary function tests

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4
Q

Amiodarone Lung

A

Usually 2-4 months at doses greater than 400 mg/day
Lipid laden foamy alveolar macrophages

Organizing pneumonia
25% of cases. Mimics infectious pneumonia

ARDS
Post surgical. Diffuse alveolar damage with interstitial pneumonitis 1-4 days post intubation.

Diffuse alveolar hemorrhage
Rare. First few days to 6 months

Solitary Pulmonary Mass
rare

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5
Q

50 year old male complains of increasing shortness of breath with exercise over the last year. Previously he has been healthy. He denies any fever, palpitations, hemoptysis, or weight loss. He denies any occupational exposure. He reports a dry cough. He does not take any medications and has no known drug allergies. He denies a smoking history. His oxygen saturation is 93% on room air. Lungs have a fine crackle pattern. Heart is regular. Examination of the extremities shows clubbing. Chest x-ray reveals diffuse linear opacities. Pulmonary function tests show a restrictive pattern. He has a decreased diffusion capacity.

Which of the following is the most likely diagnosis?

A.  Acute interstitial pneumonia
B.  Asbestosis
C.  Idiopathic cardiomyopathy
D.  Idiopathic pulmonary fibrosis
E.  Sarcoidosis
A

idiopathic pulmonary fibrosis

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6
Q

27 year old female complains of feeling short of breath recently. Her exercise tolerance has dwindled and she must rest at the top of a flight of stairs. She had been previously healthy and had attributed the change to deconditioning. She denies fever, but has an occasional dry cough. She has no allergies and does not smoke or use illicit drugs. On review of systems, she sleeps well, is able to lie flat in bed, has not had any rashes and there has been no change in bowel habits or vison. Temp 98.6 F, BP 132/68 mm Hg, pulse 88/min, and RR 18/min. O2 Sat on room air is 98% resting and 92% after 5 minutes of exercise. Spirometry is normal.

Physical examination reveals scattered crackles, but no wheezes in the lungs, normal cardiac rhythm, with no murmurs, no cyanosis, clubbing, or edema of the extremities. Chest x-ray reveals bilateral hilar lymph nodes. Purified protein derivative (PPD) is negative. Pulmonary function testing demonstrates a restrictive ventilatory defect.

Which of the following is the next most appropriate step?

1) Begin empiric antimicrobial therapy with a macrolide antibiotic
2) Obtain a transbronchial lymph node biopsy
3) Obtain a Quantiferron Gold test
4) Start her on inhaled corticosteroids

A

obtain a transbronchial lymph node biopsy

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7
Q

61 year old female with 3 day history of progressive shortness of breath, nonproductive cough, and fever. At present, the patient is able to ambulate 15 feet before becoming dyspneic. Prior she was functional and walked 2 miles in the evening after dinner with her husband. Additionally, she report one episode of hemoptysis the evening before this presentation. The hemoptysis was approximately 3 ml and maroon. She has had no prior episodes of hemoptysis and denies any lightheadedness. She has a history of SLE, and 5 years ago was diagnosed with cerebritis and lupus nephritis by renal biopsy

The patient is on prednisone and trimethoprim/sulfamethoxazole.
If pulmonary function tests reveal an increased DLCO in this patient, which of the following is the most likely diagnosis?

A.  ARDS
B.  Diffuse alveolar hemorrhage
C.  Pneumonia
D.  Pulmonary edema
E.  Pulmonary embolism

Her vital signs are: Temp 100.4F, BP 151/87 mm Hg, pulse 98/min, RR 16/min and oxygen sat of 91% on 6L O2 by nasal cannula. Chest x-ray reveals diffuse infiltrates bilaterally.

A

a couple of things can cause this

increased diffusion of co, either alveolar hemorrhage or polycythemia

asnwer is b

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8
Q

30 year old male is brought to the ER after a syncopal episode. He has not had episodes in the past. He has no fever, chills, shakes, nausea, or vomiting. He denies chest pain or palpitations. He takes no medications and has no allergies. He denies drug use. Vital signs are stable. Cardiac examination is unremarkable. Rhythm strip reveals nonsustained ventricular tachycardia. Laboratory studies are normal. Chest x-ray reveals bilateral hilar adenopathy. He has a history of a positive skin test for anergy. His serum calcium is elevated. Echocardiogram reveals segmental wall motion abnormality. He undergoes a biopsy of the myocardium and you are awaiting the results.

You correctly ascertain that upon receiving the biopsy results you will?

A. Observe at home with a holter monitor
B. Begin treatment for a disorder associated with noncaseating granulomas
C. Administer a PPD test
D. Perform a DLCO test
E. Begin therapy with antifungals for treating histoplasmosis

A

sarcoidosis elevated calcium noncaseating anergy skin test (no ppd or pos tst for candida) vtac (anything wrong with ehart)

b

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9
Q

30 year old male with a 15 pack year history of smoking. Three weeks ago he developed a URI, treated with Azithromycin.

Three days ago he developed marked SOB and a cough associated with marked hemoptysis. Examination reveals a BP of 160/95 and a RR of 20. Heart exam reveals a sinus tachycardia. His lips are cyanotic. He has 2+ pretibial edema. His BUN is 60 and Creatinine is 4.0. Urinalysis demonstrates microscopic hematuria.

Which of the following would help confirm the most likely diagnosis?

A. DLCO
B. Anti Glomerular Basement Membrane Antibody ( Anti-GBM)
C. C-ANCA
D. Alpha-1-Antitrypsin
E. Kveim test, Serum Calcium, Serum ACE levels

A

c anca

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10
Q

37 year old African American man is seen with raised red lesions on the anterior aspect of both legs. He has difficulty breathing, especially while walking at a fast pace, associated with a dry cough for the last 2-3 months. He denies fever, night sweats, weight loss, or any other symptoms. He has never smoked. BP 135/80 mm Hg, Pulse 52/min, RR 14/min. He is afebrile. Auscultation of his chest reveals discreet dry rales bilaterally with no wheezing. Heart auscultation reveals an irregular rhythm. Examination of his lower extremities shows raised red-purplish lesions on both anterior aspects of both legs. His PaO2 is 97 mm Hg at rest on room and becomes 94 mm Hg with exercise

An EKG shows episodes of second-degree AV block.

A chest x-ray reveals a diffuse bilateral reticulonodular pattern and bilateral hilar adenopathy. A bronchoscopy with transbronchial biopsy reveals noncaseating granulomas A PFT shows a decreased TLC and RV with an FEV1/FVC of 95%of predicted. Laboratory studies show minimally elevated calcium and ACE levels. Other lab studies are normal.

After you review this patient’s clinical presentation and findings, which of the following is the most appropriate treatment plan at this time?
A. Begin therapy with high-dose systemic corticosteroids
B. Follow ACE levels, Chest x-rays, and O2 sats, and employ “watchful waiting”
C. Place a transvenous pacemaker
D. Start treatment for TB
E. Start an appropriate antibiotic regimen accepted for this condition

A

a sarcoidosis

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11
Q

75 year old male comes to the office complaining of severe dyspnea that has been ongoing for the past 1 year. He denies a cough, chest pain, hemoptysis, or weight loss. He has a significant smoking history of two pack per day for the past 50 years. He has no other medial issues. He has no allergies and takes no medications
He worked as a stone engraver until 10 years ago when he retired. His vital signs are stable. Pulmonary examination reveals end expiratory crackles bilaterally. He has clubbing. His chest x-ray reveals multiple sub centimeter nodules and eggshell calcifications of hilar lymph nodes.

Which of the following is the most likely diagnosis

A.  Adenocarcinoma
B.  Asbestosis
C.  Idiopathic pulmonary fibrosis
D.  Silicosis
E.  Tuberculosis
A

D

egg shell cacifications are pathenemonic for this

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12
Q

50 year old female presents with acute dyspnea. Her symptoms began with dry cough, shortness of breath, malaise, and fever seen days earlier. She is brought to the ER in acute hypoxemic ventilatory failure. pH 7.30, PaCO2 65, PaO2 55 on 100% FiO2 intubated and on ventilator.
Her chest x-ray demonstrates diffuse alveolar infiltrates and air space consolidation suggestive of ARDS.
A CT scan reveals bilateral air apace consolidation with areas of ground glass opacities with little honeycombing. Septal thickening and subpleural distribution of the opacities is noted

A lung biopsy reveals diffuse alveolar damage.

She is treated with mechanical ventilation, steroids, and antibiotics. She dies two days later.

Which of the following is the most likely diagnosis?

A.  Acute interstitial pneumonia
B.  Asbestosis
C.  Idiopathic cardiomyopathy
D.  Idiopathic pulmonary fibrosis
E.  Sarcoidosis
A

A, rapid, sever hypxia, ards on xray

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13
Q

49 year old man has a chest x-ray as part of a pre-op workup before gastric bypass surgery. The surgeon who reviews the film is concerned because there appear to be small nodules in the lateral aspects of the left lung field. A high resolution CT scan is ordered, which further defines these nodules.

After review by the radiologist, the opacities seen on chest radiograph are felt to be pleural-based. At least eight focal areas of pleural plaques are visible, as well as areas of diffuse pleural thickening, subpleural linear densities, and areas of basilar fibrosis. Although the patient states that he has no respiratory complaints and he never smokes, a set of pulmonary function tests reveal a borderline restrictive pattern and a diminished diffusion capacity of the lung for carbon monoxide (DLCO)

Which of the following aspects of this patient’s history is most likely to explain these abnormal findings?
A.  Dietary/nutritional review
B.  Family medical history
C.  Occupational history
D.  Review of symptoms
E.  Travel history
A

first thought is asbestosis, that is rigth so answer is C

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14
Q

37 year old male presents with 2-3 weeks of increasing dyspnea, occasional hemoptysis, sinusitis, and on episode of epistaxis. Renal function is normal. His UA reveals 10-15 RBCs and 2 WBCs. His chest x-ray demonstrates bilateral nodular infiltrates. One is cavitary.

Which of the following is true?
A. His diagnosis is most likely Tuberculosis
B. His diagnosis is most likely Goodpastures syndrome
C. He will have a positive test for c-ANCA
D. He will have an elevated ACE level
E. He will soon develop congestive heart failure

A

c anca wegeners

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15
Q

27 year old female presents to the ER with cough, fever, dyspnea, weight loss, malaise, and night sweats for the past week. She complains of recent onset of wheezing during this time as well. Her CBC demonstrates a marked eosinophilia with over 35% eosinophils. Her chest x-ray demonstrates peripheral, nonsegmental alveolar infiltrates and possible non-cavitating lung lesions. You suspect asthma and a superimposed infection. You treat her with albuterol by inhalation and large doses of oral corticosteroids. The infiltrates on the chest x-ray resolve in 2 days and she becomes asymptomatic.

She is sent home and returns to the ER in three weeks with the same symptoms. She has also now developed symptoms of diarrhea and abdominal pain with diarrhea.

Your correct diagnosis is?
A.  Asthma with associated mucus plugs and atelectasis
B.  Bronchiectasis
C.  Chronic eosinophilic pneumonia
D.  Churg – Strauss Syndrome
E.  Goodpasture’s variant
A

c and both have eosinophilia

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16
Q

Patient is a 50 year old female that presents with increased difficulty breathing, cough, and exertional dyspnea. She is a non-smoking housewife. She is married. Her husband is a wood worker and fixes / remodels old buildings and warehouses for a living. Physical exam demonstrates bibasilar fine crackles on auscultation along with the presence of clubbing. Chest x-ray shows basilar opacities and bilateral calcified pleural plaques.

Based upon the history and these findings, you expect to diagnose?

A.  Idiopathic pulmonary fibrosis
B.  Asbestosis
C.  BOOP
D.  Kaplan’s syndrome
E.  Collagen vascular disease of the lung
A

asbestosis

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17
Q

65 year old male that has been retired for the past four years. He is sent to you for evaluation because of an abnormal chest x-ray. As you review the x-ray you note that there are rounded opacities, 1-5 mm in size in the upper lung zones. Egg-shell calcifications are noted in the region of the hilar and mediastinal lymph nodes. He tells you that he has been having increasing SOB for the last 2 years. He is thin and using accessory muscles of respiration. BP is 140/80, Pulse 90 and regular, Lung sounds exhibit decreased flow and some fine crackles at the end of expiration.

Based upon your presumptive diagnosis, you correctly :

A. Apply a PPD intermediate skin test
B. Place this patient on a Beta 2 agonist
C. Place this patient on inhaled corticosteroids
D. Start him on chemotherapy
E. Order an echocardiogram

A

a he has silicosis and you cant treat it but he is susceptivle to tb

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18
Q

65 year old male who retired to Pueblo, CO after working the mines of West Virginia for twenty-five years. Over the years he has had increasing difficulty with shortness of breath. He can no longer walk up the stairs to his bedroom, and now sleeps on the living room sofa. Physical exam reveals right-sided heart failure with 2+ pretibial edema, a prolonged expiratory phase, and diffuse wheezing

The underlying pathology in this patient is:
A. Localized fibrous plaques or, rarely, diffuse pleural fibrosis
B. Coalescence of particle containing macules that form discrete areas of interstitial fibrosis causing distention of the respiratory bronchioles, forming focal areas of emphysema.
C. The development of noncaseating granuloma formation.
D. Fibrosis secondary to the effects of anti-GBM antibody
E. The development of chronic mucopurulent infections causing dilation of the respiratory bronchioles

A

b

sleeping downstairs bc he is too short of breath

coalwerkers pneumoconiosis

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19
Q

35 year old coal miner that has a history of rheumatoid arthritis. He is being treated with Methotrexate, gold injections, and Aspirin. Your are asked to consult based upon an abnormal chest x-ray that demonstrates multiple calcified pulmonary nodules throughout the lung fields bilaterally. The presence of a pleural effusion is also noted in the left lower lung field.

You correctly diagnose:

A.  Silicosis
B.  Caplan’s syndrome
C.  Sarcoidosis
D.  Miliary Tuberculosis
E.  Coal Workers Pneumoconiosis
A

b

arthritis causes

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20
Q

47 year old roofer from Malawi who is seeing you because of increased shortness of breath of increasing duration. He smokes 1 pack of “Lucky Strike” cigarettes daily and has done so for the last thirty years. He has been in the US for the last two years and now works in the roofing industry here in Colorado. He has a chronic non productive cough. His chest x-ray demonstrates small, irregular, shadows in lower lung zones along with thickened pleural calcified plaques present under diaphragms and lateral chest wall.

Physical exam reveals fine end respiratory crackles heard more predominantly in the lung bases bilaterally and digital clubbing is noted.
Pulmonary function testing shows a decreased vital capacity, decreased total lung capacity, and a decreased DLCO.

You expect to find which of the following on lung biopsy?
A. Caseating granulomas
B. Discrete pale nodules in the upper zones of the lungs that have coalesced into hard, collagenous scars.
C. Golden brown, fusiform rods with a translucent center consisting of particulate fibers coated with an iron-containing proteinaceous material
D. A lymphocytic alveolitis leading to pulmonary fibrosis
E. Lymphocytes, plasma cells, and macrophage aggregates resulting in interstitial fibrosis and obliterative bronchiolitis

A

c

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21
Q

64 year old male with a chief complaint of increasing SOB, a 20 lb weight loss over the last three months, and non pleuritic chest pain.
On examination he has dullness to percussion on the right lung base and bilaterally diminished breath sounds that is more pronounced on the right. He has positive JVD, distant heart sounds, and a pulsus paradoxus of 18 mm. There is low voltage on the EKG

Chest x-ray reveals a nodular, irregular pleural thickening noted on the right side with a right sided pleural effusion and a pericardial effusion with a greatly enlarged heart. He has never smoked. He immigrated to the United States from Ireland where he was employed as a ship builder and “shipyard worker for 50 years. He has helped build battle ships, cruise ships, and heavy freighters.

You perform a thoracentesis to retrieve pleural fluid for diagnostic purposes, expecting to find:
A. Pleural fluid that stains positive for Acid Fast Bacilli.
B. Pleural fluid analysis with an uncharacteristically low random sugar.
C. Pleural fluid analysis compatible with a transudate as seen in CHF
D. Pleural fluid analysis with beryllium residue
E. Pleural fluid analysis with cells compatible with malignant mesothelioma

A

E

may have to do pleural biopsy

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22
Q

Light Criteria for Exudate

A
  1. Pleural fluid protein/serum protein > 0.5
  2. Pleural fluid LDH/Serum LDH > 0.6
  3. Pleural fluid LDH more than two-thirds normal upper limit for serum
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23
Q

35 year old male who has a complaint of progressive dyspnea on exertion, anorexia, night sweats, and a 10 lb weight loss over the last five months. He is employed as a nuclear technician at a power plant in Louisiana. Because of hurricane Katrina, he evacuated La, and is now in Fort Worth. On examination, he has mildly decreased breath sounds bilaterally. The remainder of the examination is normal. Chest x-ray examination reveals bilateral fibrosis with marked bilateral hilar adenopathy. He was previously diagnosed as having sarcoidosis. You review his chart and note that he has positive skin tests to mumps and trichophyton, a normal serum ACE level, and a normal serum calcium.

Because you are a “sharp clinician” you correctly:
A. Perform a pleural biopsy looking for asbestosis
B. Perform a BAL for a beryllium lymphocyte proliferation test
C. Perform a bronchoscopy looking for a non-caseating granuloma.
D. Perform a BAL looking for ACE levels in the aspirate
E. Perform a parotid gland biopsy for Heerfordt’s syndrome

A

b

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24
Q

Heerfordt’s disease

A

A variant of Sarcoidosis

Characterized by nonsuppurative parotitis, uveitis, mild fever, and facial nerve paralysis

25
Q

25 year old male who has recently immigrated from Sri Lanka. He complains of dry cough, malaise, episodic fevers, and intermittent wheezing. These symptoms are worse at night.
He has lost 25 pounds over the last 6 months.
On his CBC he has a marked eosinophilia with an absolute eosinophil count that is 2000 eosinophils/ml. His IGE level is markedly elevated. His Chest x-ray shows a diffuse infiltrate with multiple nodules. His sedimentation rate is 40. Charcot-Leyden crystals are seen in his sputum specimen.

Based upon your suspected diagnosis, you correctly treat him with?
A.  Corticosteroids
B.  Albuterol
C.  Diethylcarbamazine
D.  Azithromycin
E.  Isoniazid
A

think parasites in asia and africa

C used for parasites

Wuchereria bancrofti
Elephantiasis

26
Q

14 year old female with cough and wheezing, transient pulmonary infiltrates, and blood eosinophilia. When she has the episodes of wheezing her eosinophil count is markedly elevated and she runs temperatures as high as 100F. Her fever and episodes of wheezing resolve in 3-4 days and she then becomes asymptomatic. Her WBC count is 15,000 during and attack with 40% eosinophils.

With this most recent episode, she also presents with abdominal pain, nausea, vomiting, and x-ray evidence of an acute GI obstruction.  You correctly diagnose?
A.  Churg-Strauss Syndrome
B.  Loeffler’s Syndrome
C.  Allergic aspergillosis
D.  BOOP
E.  Sarcoidosis Pulmonary Variant
A

b

27
Q

38 year old female who was diagnosed and treated for non-metastatic breast cancer 16 months ago. Her treatment consisted of a right mastectomy that went well and radiation therapy that ended 12 months ago. She now complains of a low-grade fever, night sweats, dyspnea on exertion, increased sputum production, and occasional cough. Her O2 sat level is 92%.

You correctly expect that?
A. She will have had chronic remodeling of her lung tissue resulting in pulmonary fibrosis
B. She now demonstrates lymphangitic spread of her primary tumor.
C. She now has an opportunistic infection secondary to her altered state of immunity
D. She will develop bronchiectasis
E. She will require bronchodilator therapy.

A

a from radiation therepy

radiate with hodgkins and htey try to shield heart and lungs

radiating pneuomonities causes pulmonary fibrosis

this can cause fever

28
Q

50 year old male with a history of sinusitis, allergies, and severe persistent asthma for the past ten years. He is on SABA’s, LABA, inhaled steroids, cromolyn, and the leukotriene inhibitor, singulair.
He now presents with marked respiratory difficulty, a neuritic pain in his legs, arms, and hands. His skin demonstrates erythematous maculopapules resembling erythema multiforme. He has marked abdominal pain with rebound on exam. He also reports decreased urination.

His chest x-ray demonstrates marked right sided infiltrates, bilateral patchy infiltrates, and areas with diffuse nodular infiltrates. His eosinophil count is also markedly elevated with 25% of his cells being eosinophils. p-ANCA levels are elevated. His IgE level is elevated. His BUN and creatinine are elevated.

Which of the following is the most likely diagnosis?
A.  Wegener’s granulomatosis
B.  Churg-Strauss syndrome
C.  Desquamative interstitial fibrosis
D.  Sarcoidosis – Stage III
E.  Loeffler’s Syndrome
A

systemic acting all over the body

b

29
Q

27 year old ranch hand brought in with the onset of severe respiratory distress. He is one of the three patients brought into the ER with similar symptoms. He was working at the farm doing generalized cleaning, and had this sudden onset

You correctly diagnose?
A. Farmer’s lung secondary to exposure to Thermophilic Actinomycetes
B. RADS (Reaactive Airways Dysfunction Syndrome)
C. Silo Filler’s Disease
D. Strep Pneumonia

A

c

30
Q

prednisone is used for allergic

A

allergic aspergillous and treat with itraconazole

31
Q

acute interstitial fibrosis does not have what on xray

A

nodules

32
Q

renal sinus and lung

A

wegeners

33
Q

methacholine challenge test diagnoses

A

asthma

34
Q

acute interstitial pneumonia come on

A

fast

35
Q

dyspnea is number one symptom and it was slow onset and he fits the age 50-60

A

idiopathic pulmonary fibrosis

36
Q

sarcoidosis symptoms

A

hilar adenopathy

elevated ace

vitd and calcium

ereythem nodosum

37
Q

sarcoidosis lymph node biopsy

A

bialteral hilar lymph nodes - could be lymphoma, lymphangioleomyomatosis (would see cysts not lymphadnopathy)

bc patient has sarcoidosis

38
Q

increased dlco

A

a couple of things can cause this

increased diffusion of co, either alveolar hemorrhage or polycythemia

39
Q

elevated calcium noncaseating anergy skin test (no ppd or pos tst for candida) vtac (anything wrong with eha

A

sarcoidosis

40
Q

red purplish sarcoidosis lesions

A

erythema nodosa seeen with sarcoidosis and coccidiomycoses

cant diagnose sarcoidosis by biopsing these lesions

41
Q

egg shell cacifications are pathenemonic for this

A

silicosis

42
Q

idiopathic pulmonary fibrosis has a? course

A

slower

43
Q

churg strauss syndrome

A

diarrhea and gi issues can affect lungs and kidneys get better with steroids and then comes back

44
Q

chronic mucopurulent infections causing dilation of respiratory bronchioles

A

bronchiectasis

45
Q

caseating granulomas

A

tb

46
Q

discrete pale noudles in the upper zones of the lungs that have coalesced into hard collagenous scars

A

silicosis usually upper lobe

47
Q

goldern brown, fusiform rods with a translucent center consisting of particulate fibers coated with an iron-containing proteinaceous material

A

feruginous or asbestos bodies

48
Q

lymphocytes plasma cells and macrophoage aggregates resulting in interstitial fibrosis and obliterative bronchiolitis

A

cop

49
Q

pleural fluid analysis with an uncharactertically low random sugar

A

rheumatoid arthritis

50
Q

bal for a beryllium lymphocyte proliferation test

A

looks a lot like sarcoidosis

51
Q

parotid gland biopsy for heerfordts syndrome

A

sarcoidis with swollen parotic gland and facial nerve paralysis

52
Q

wuchereria bancrofti, elephantiasis lung phase

A

causes eosinophilia and cough and wheezing

53
Q

loefflers syndrome

A

ascaris infection with lung phase caues eosinophle cough and then you swallow and it oes to gi trat to cause obstruction

54
Q

lymphangitic spread of tumor

A

would have enlarged lymph node

55
Q

desquamative interstitial fibrosis

A

wouldve smoked

wont get systemic

56
Q

sarcoidosis shows

A

hilar adeonpathy

57
Q

farmers lung is what type of process?

A

slow

58
Q

silo fillers disease

A

nitrogen dioxide from silo not properly ventilated