Case Reports in Medicine

Case Reports in Medicine / 2009 / Article

Case Report | Open Access

Volume 2009 |Article ID 941258 | 6 pages |

Hypersensitivity Vasculitis with Leukocytoclastic Vasculitis Associated with Alpha-1-Proteinase Inhibitor

Academic Editor: Klaus F. Helm
Received18 Oct 2009
Accepted18 Nov 2009
Published24 Feb 2010


Prolastin is a commercially available form of alpha-1-antitrypsin (AAT) that is derived from pooled human plasma and used for treatment of severe alpha-1-antitrypsin deficiency (AATD). We describe a patient with AATD who developed presumed hypersensitivity vasculitis (HV) following a Prolastin infusion. Hypersensitivity vasculitis (HV), or cutaneous vasculitis, is characterized by inflammation of the small vessels of the skin with resultant ischemia to the distally supplied areas. To our knowledge, this is the first reported case of presumed hypersensitivity vasculitis following Prolastin infusion.

1. Case Report

A-56-year old woman with a background history of type 2 diabetes, hypertension, GERD, severe asthma, COPD, and newly diagnosed alpha-1-antitrypsin deficiency (AATD) (ZZ phenotype) acutely developed shortness of breath and fatigue following her first Prolastin infusion. A week later she received a second infusion with premedication. Over the following 3 weeks the patient complained of a constellation of symptoms including dyspnea, wheezing and one episode of hemoptysis. She also complained of nonspecific arthralgias and a diffuse rash. During this time she was admitted to her home hospital where she was treated with steroids and antibiotics (Augmentin). She did not improve and was subsequently transferred to Mayo Clinic for further evaluation.

The initial evaluation revealed the following: temperature, C; blood pressure, 132/78; pulse rate, 73; oxygen saturations, 98% on 3 L/min nasal cannula; and respiratory rate, 18. She was alert and oriented and sitting comfortably in no apparent distress with a cushingoid appearance (due to steroid use for chronic asthma and COPD). Physical exam revealed multiple palpable purpuric violaceous papules coalescing into serpiginous plaques with large adherent black eschars overlying her upper and lower extremities. Several punched out ulcerations with yellow fibrinous adherent material were present over her bilateral upper thighs and buttocks (Figure 1). Lung exam revealed bibasilar crackles. Remainder of her exam was normal. A complete list of her medications is included in Table 2.

Laboratory studies showed a normocytic anemia, slight leucocytosis, elevated sedimentation rate, C-reactive protein, and low AAT (Table 1). Urinalysis was unremarkable. CT chest showed consolidative infiltrates in the left lower lung posteriorly and scattered alveolar infiltrates throughout both lungs. Bronchoscopy revealed old blood in the R lower lobe subsegmental bronchus without any other endobronchial lesions. BAL had a bloody return which cleared suggestive of prior bleeding. Skin punch biopsy of the left lower leg revealed mild superficial dermal perivascular neutrophilic inflammation. Direct immunofluorescence of the skin biopsy was negative for deposits (IgG, IgM, IgA, C3, and fibrinogen all negative). She was treated with prednisone 60 mg orally once a day, dapsone 100 mg by mouth orally once a day for Pneumocystis jiroveci pneumonia prophylaxis as she had a sulfonamide allergy, daily whirl pool therapy, and topical therapy with Sweitzer solution (zinc-boron-salicylate solution) and 0.1% triamcinolone cream. Her skin lesions and associated symptoms continued to improve with treatment.

Laboratory nameLaboratory ResultReference Ranges

Hemoglobin11.013.5–17.5 g/dL
Mean Corpuscle volume90.281.6–98.3 FL
Leukocyte count13.1 3.5–10.5×109/L
Platelet count222150–450 ×109/L
Creatinine0.60.6–1.1 mg/dL
Blood Urea Nitrogen266–21 mg/dL
Sedimentation rate300–22 mm/Lh
C-Reactive Protein23.9<= 8.0 mg/L
Myeloperoxidase Ab< 3.0< 6.0 U/mL
Proteinase 3 antibody< 3.0< 3.0 U/mL
Complement total6330–75 u/mL
Complement C1q1712–22 mg/dL
C3 Complement15075–175 mg/dL
C4 complement2014–40 mg/dL
Antinuclear Ab0.9<= 1.0 U
Anti DS DNA IgG< 1.0< 5.0 iu/mL
SS-A/RO Ab IgG< 0.2> or = 1.0 U
SS-B/LA IgG0.4> or = 1.0 U
Jo 1 Ab IgG0.2> or = 1.0 U
Scl 70 Ab IgG< 0.2> or = 1.0 U
Cyclic citrullated peptide< 15.6< 20 U
Anti glomerular basement membrane< 1.0<= 20.9 U
Alpha 1-anti-trypsin level23100–190 mg/dL
IgA24150–400 mg/dL
Hepatitis B antibodyNegative
Hepatitis Be antigenNegative
Hepatitis B antigenNegative
Hepatitis C antibodyNegative
Hepatitis C RNA detect/quantNegative


Albuterol/ipratropiumQ 4 hrs as needed for SOB
Alprazolam0.5 mg by mouthDaily at bedtime
Ascorbic Acid1000 mg by mouthDaily at bedtime
BupropionUnknown doseAt bedtime
Calcium/Vitamin D500 mg/250 units by mouthTwice a day with meals
Fluticasone/Salmeterol500/50 discus inhalationTwice a day
Furosemide40 mg by mouthDaily in am
Gabapentin600 mg by mouth in am, 600 mg at noon, 1200 mg at bedtimeThree times a day
Glucosamine/Chondroitin500 mg/400 mg by mouthDaily
Guaifenesin SR600 mg by mouthTwice a day
Ipratropium MDIQ 4–6 hrs as needed
Loratadine10 mg (during allergy season)Daily
Magnesium oxide400 mg by mouthDaily with breakfast
Montelukast10 mg by mouthAt bedtime
Multivitaminone tablet by mouthDaily in am
Nasonex1 spray to each nostrilAt bedtime
Omega 31000 mg by mouthTwice a day
Omeprazole20 mg by mouthDaily
Zoloft100 mg by mouthDaily
Sucralfate1 gram by mouth Four times a day before meals and at bedtime
Verapamil SR240 mg by mouthDaily in am

2. Discussion

Alpha-1-antitrypsin (AAT) is a 394 amino acid glycoprotein produced by the liver and normally found in the serum and extravascular locations, including the alveolar lining of the lung. The main function of AAT is inhibition of neutrophil elastase. If the quantity or functional activity of AAT is significantly reduced, the resulting imbalance leaves the alveolar walls susceptible to proteolytic damage, resulting in emphysema [1]. The association between AATD and heritable emphysema was discovered in 1963 [2, 3]. Subsequent epidemiologic evidence suggested that a serum AAT level of 11  mol/L (80 mg/dL), which is 35% of the normal level, represents a “threshold” value below which the risk of developing emphysema is significantly increased [1]. The ability to isolate and purify the AAT protein from human blood has made augmentation therapy possible. Augmentation therapy has been shown to raise antiprotease serum and epithelial lining fluid levels above the “protective threshold” value. Evidence suggests that this approach slows the decline in lung function, could reduce infection rates, might enhance survival, and is well tolerated [4]. Based on available evidence, the American Thoracic Society recommends augmentation therapy for individuals with both a documented severe deficiency of AAT and fixed airflow obstruction [1]. Prolastin, a commercial preparation of AAT from pooled blood, is given by intravenous infusion at a dose of 60 mg/kg ideal body weight once a week. The largest cohort study in the USA looking at side effects was conducted by the National Heart Lung and Blood institute (NHLBI) AATD Registry Group. The most frequent reported side effects include headache, dizziness, nausea, and dyspnea [5]. Although acute allergic reactions, including anaphylaxis, have been reported, these events are rare. It is important to be aware that patients with severe AAT deficiency may also be IgA deficient and that Prolastin contains some IgA [5].

Possible differentials for this patient’s skin findings are discussed below. Necrotizing panniculitis, which is characterized by inflammatory lesions of the skin and subcutaneous tissue, is the major dermatologic manifestation of AATD [69]. AATD individuals generally present with a hot, painful, red subcutaneous nodule or plaque on the thigh or buttocks [10]. These lesions can be difficult to distinguish from panniculitis due to other causes, but may be more inflammatory with an oily yellow discharge and more pronounced histologic evidence of acute inflammation. Panniculitis is the least common of the well-recognized complications of AAT deficiency, with fewer than 50 cases reported in the English literature [6, 913]. The prevalence among AAT-deficient subjects is probably less than one case per thousand. Panniculitis has been reported to occur in a variety of phenotypes, including and Seventy percent of reported cases have occurred in patients with phenotype and severe AAT deficiency [10]. Similar to the pathophysiology of emphysema in such individuals, the panniculitis is thought to result from unopposed proteolysis in the skin. Deep excisional biopsies may be required to establish the diagnosis. Characteristic histologic findings include lobular fat necrosis of the lower reticular dermis, with abundant neutrophil influx interspersed with normal-appearing fat and necrotic panniculus [14]. Based upon this presumed pathophysiologic mechanism of unopposed proteolysis, treatment of panniculitis in AATD subjects has focused on restoring antiprotease activity. Intravenous infusion of purified AAT has ameliorated the panniculitis in some patients [7, 10]. Other treatments have included dapsone (100 mg/day for several weeks) and doxycycline (200 mg/day for as long as several months) [7, 10, 12]. The latter is believed to act by scavenging reactive oxygen species produced by neutrophils and/or by slowing the breakdown of matrix proteins by elastase. Of note the appearance of these skin findings in this case is not classic for panniculitis.

Wegener’s Granulomatosis, which is a systemic vasculitis of the medium and small arteries and the venules and arterioles, can have dermatological manifestations. These include vesicular, palpable purpuric, ulcerative, and hemorrhagic lesions. This patient’s presentation and clinical findings are not compatible with the American College of Rheumatology criteria for the classification of Wegener's granulomatosis [15]. In particular, there was no upper airway involvement, no evidence of granulomatous inflammation on her biopsy, no abnormal urinary sediment or renal involvement, and negative PR3 and MPO antibodies.

Likewise this patient’s presentation and findings are not compatible with Churg-Strauss syndrome (CSS), also called allergic granulomatosis and angiitis. This multisystem disease is characterized by allergic rhinitis, asthma, and prominent peripheral blood eosinophilia, none of which were present in this case. Two-thirds of patients with CSS have skin lesions, which usually appear as subcutaneous nodules on the extensor surfaces of the arm, particularly the elbows, hands, and legs [16]. The skin lesions can appear as palpable purpura, macular or papular erythematous rash, hemorrhagic lesions, ranging from petechiae to extensive ecchymoses, tender cutaneous or subcutaneous nodules in which granulomas are usually found on biopsy.

Hypersensitivity vasculitis (HV) or cutaneous vasculitis is characterized by inflammation of the small vessels of the skin with resultant ischemia to the distally supplied areas [6]. In 1990 the American College of Rheumatology proposed the following five criteria for the classification of hypersensitivity vasculitis:

(1)age >16,(2)use of possible offending drug in a temporal relation to the symptoms,(3)palpable purpura,(4)maculopapular rash,(5)biopsy of skin lesion showing neutrophils around an arteriole or venule.

The presence of three or more of these criteria had a sensitivity and specificity for the diagnosis of hypersensitivity vasculitis of 71 and 84 percent, respectively [4]. Leukocytoclastic vasculitis (LV) is a histologic diagnosis. It involves the deposition of immune complexes in vessel walls, ultimately leading to cellular infiltrates, cytokine release, and vessel damage. If IgA deposition is noted on skin biopsy, it is necessary to rule out Henoch-Schönlein purpura. Immunofluorescence can be used if the skin biopsy is inconclusive. Common causes of HV include drugs, infections (HIV, hepatitis B and C), malignancy, connective tissue disease (SLE, RA), and autoimmune disease. The most common offending drugs include antibiotics (penicillins, cephalosporins, and macrolides), loop and thiazide diuretics, sulfonamides, allopurinol, and phenytoin [17]. The major clinical findings of HV in addition to the skin lesions, palpable purpura and/or petechia, include fever, urticaria, arthralgias, lymphadenopathy, low serum complement levels, and an elevated erythrocyte sedimentation rate. In most patients, these symptoms and/or findings begin from 7 to 10 days after antigen exposure, the time required to produce a sufficient quantity of antibody to produce antigen-antibody complexes [18, 19]. However, the latent period may be as short as two to seven days with a secondary antigen exposure or longer than two weeks with a long-acting drug such as benzathine penicillin [20]. The initial laboratory work-up for evaluation of small vessel vasculitis has been suggested to include complete blood count, erythrocyte sedimentation rate, urinalysis, chemistry panel, stool guaiac, ANA, ANCA, Rheumatoid factor (RF), cryoglobulins, C3, C4, serology for hepatitis B and C, chest X-ray, and skin biopsy [21]. Skin biopsy with specimens for routine light microscopy and direct immunofluorescence examination is the first step in determining whether authentic vasculitis is present and excluding pseudovasculitic disorders (e.g., warfarin necrosis, cholesterol emboli). The choice and timing of the biopsy will affect diagnostic yields. Early lesions, less than 48 to 72 hours old, are more likely to yield neutrophilic vasculitis, whereas older lesions are more likely to show a solely perivascular lymphocytic infiltrate without evidence of vessel damage. Additional tests to consider include blood cultures and echocardiography if the patient has a high fever and/or has a heart murmur and anti-streptolysin O titers in children [22]. The treatment options include discontinuation of the inciting drug or antigen which should lead to resolution of the signs and diagnosis within a period of days to a few weeks. Conservative measures include rest, leg elevation, support hoses, avoiding cold exposure and tight fitting clothes [23]. Treatment of the underlying infection, such as the administration of interferon and ribavirin to those with hepatitis C virus and cryoglobulinemia, is recommended. In patients with more severe or persistent cutaneous disease not due to infection, drugs such as colchicine, antihistamines, and dapsone may be helpful [2426]. Occasionally, combinations of these drugs (e.g., dapsone and pentoxifylline) are more effective than single therapy [27]. Patients with complicated or systemic disease in whom more toxic therapies are required should be referred to a rheumatologist for consultation. Immunosuppressive therapy with corticosteroids or cytotoxic agents should be reserved for the infrequent patient with fulminant or progressive disease, some of whom may have microscopic polyarteritis [26]. Novel therapy includes TNF-alpha inhibitors, intravenous immunoglobulins, or plasmapheresis [23]. Rechallenge of the suspected drug is not recommended.

Here we describe a patient who developed HV 2 weeks following her 2nd Prolastin infusion with fulminant skin disease. As mentioned previously drugs are the most common offending agents, but drug-induced vasculitis is a diagnosis of exclusion. It is hypothesized that drugs act as haptens that cause an immune response. The most common medications include antibiotics (penicillins, cephalosporins, macrolides), antiretrovirals, granulocyte colony-stimulating factor, loop and thiazide diuretics, sulfonamides, allopurinol, and phenytoin [28]. Furosemide, a medication reported to cause HV in a limited number of case based reports, was a stable medication for this patient and therefore unlikely to be implicated in her condition [29, 30]. Another important factor to consider is that Prolastin contains trace amount of polyethylene glycol (PEG), and other medications mixed with PEG have been reported to cause HV (such as PEG interferon for Hepatitis C). It is possible that this patient’s reaction was secondary to the Prolastin preparation due to PEG instead of the alpha-1-antitrypsin protein itself. Zemeira, which is another preparation for AAT augmentation, does not contain PEG and could be used if a true reaction to PEG was verified. Due to the temporal relationship of the rash with the Prolastin infusion and no other new medications, we believe that the Prolastin is the cause of the vasculitis. To our knowledge this is the first reported case of HV secondary to Prolastin administration. Physician and other healthcare professionals should be aware of the possible rare adverse reaction using Prolastin.


COPD:Chronic obstructive pulmonary disease
ANCA:Antineutrophil cytoplasmic antibody
TNF:Tumour necrosis factor
RF:Rheumatoid factor
AATD:Alpha-1-antitrypsin deficiency
HV:Hypersensitivity vasculitis
LV:Leukocytoclastic vasculitis
HIV:Human immunodeficiency virus
SLE:Systemic lupus erythematosus
RA:Rheumatoid arthritis
PeG:Polyethylene glycol
CSS:Churg-Strauss syndrome
SOB:Shortness of breathe.


  1. H. Wiedemann and J. Stoller, “Lung disease due to alpha 1 anti-trypsin deficiency,” Current Opinion in Pulmonary Medicine, vol. 2, no. 2, pp. 155–160, 1996. View at: Google Scholar
  2. C. B. Laurell and S. Ericksson, “The electrophoretic alpha 1 globulin pattern of serum in alpha 1 anti-trypsin deficiency,” Scandinavian Journal of Clinical & Laboratory Investigation, vol. 15, pp. 132–140, 1963. View at: Google Scholar
  3. S. Eriksson, “Pulmonary emphysema and alpha 1 antitrypsin deficiency,” Acta Medica Scandinavica, vol. 175, pp. 197–205, 1964. View at: Google Scholar
  4. L. H. Calabrese, B. A. Michel, D. A. Bloch et al., “The American College of Rheumatology 1990 criteria for the classification of hypersensitivity vasculitis,” Arthritis and Rheumatism, vol. 33, no. 8, pp. 1108–1113, 1990. View at: Google Scholar
  5. I. Petrache et al., “Safety and efficacy of alpha-1-antitrypsin augmentation therapy in the treatment of patients with alpha-1-antitrypsin deficiency,” Biologics: Targets & Therapy, vol. 3, pp. 193–204, 2009. View at: Google Scholar
  6. J. K. Stoller and L. S. Aboussouan, “Alpha-1-antitrypsin deficiency,” The Lancet, vol. 365, no. 9478, pp. 2225–2236, 2005. View at: Google Scholar
  7. M. R. Pittelkow, K. C. Smith, and W. P. D. Su, “Alpha-1-antitrypsin deficiency and panniculitis. Perspectives on disease relationship and replacement therapy,” American Journal of Medicine, vol. 84, no. 6A, pp. 80–86, 1988. View at: Google Scholar
  8. B. K. Edmonds, J. A. Hodge, and R. L. Rietschel, “Alpha1-antitrypsin deficiency-associated panniculitis: case report and review of the literature,” Pediatric Dermatology, vol. 8, no. 4, pp. 296–299, 1991. View at: Google Scholar
  9. J. K. Strolo and M. Piliang, “Panniculitis an alpha-1-antitrypsin deficiency,” Clin. Pulm. Med., pp. 15–113, 2008. View at: Google Scholar
  10. P. Geraminejad, J. R. Debloom II, H. W. Walling, R. D. Sontheimer, and M. Vanbeek, “Alpha-1-antitrypsin associated panniculitis: the MS variant,” Journal of the American Academy of Dermatology, vol. 51, no. 4, pp. 645–655, 2004. View at: Publisher Site | Google Scholar
  11. C. Irvine, V. Neild, C. Stephens, and M. Black, “Alpha-1-antitrypsin deficiency panniculitis,” Journal of the Royal Society of Medicine, vol. 83, no. 11, pp. 743–744, 1990. View at: Google Scholar
  12. T. Sorsa, O. Lindy, Y. T. Konttinen et al., “Doxycycline in the protection of serum alpha-1-antitrypsin from human neutrophil collagenase and gelatinase,” Antimicrobial Agents and Chemotherapy, vol. 37, no. 3, pp. 592–594, 1993. View at: Google Scholar
  13. K. O'Riordan, A. Blei, M. S. Rao, and M. Abecassis, “α1-antitrypsin deficiency-associated panniculitis: resolution with intravenous α1-antitrypsin administration and liver transplantation,” Transplantation, vol. 63, no. 3, pp. 480–482, 1997. View at: Publisher Site | Google Scholar
  14. “American Thoracic Society/European Respiratory Society statement: standards for the diagnosis and management of individuals with alpha-1 antitrypsin deficiency,” American Journal of Respiratory and Critical Care Medicine, vol. 168, pp. 818–900, 2003. View at: Publisher Site | Google Scholar
  15. R. Y. Leavitt, A. S. Fauci, D. A. Bloch et al., “The American College of Rheumatology 1990 criteria for the classification of Wegener's granulomatosis,” Arthritis and Rheumatism, vol. 33, no. 8, pp. 1101–1107, 1990. View at: Google Scholar
  16. R. A. Schwartz and J. Churg, “Churg-Strauss syndrome,” British Journal of Dermatology, vol. 127, no. 3, pp. 199–204, 1992. View at: Google Scholar
  17. R. Blanco, V. M. Martínez-Taboada, V. Rodríguez-Valverde, and M. García-Fuentes, “Cutaneous vasculitis in children and adults: associated diseases and etiologic factors in 303 patients,” Medicine, vol. 77, no. 6, pp. 403–418, 1998. View at: Publisher Site | Google Scholar
  18. L. H. Calabrese and G. F. Duna, “Drug-induced vasculitis,” Current Opinion in Rheumatology, vol. 8, no. 1, pp. 34–40, 1996. View at: Google Scholar
  19. R. Y. Leavitt and A. S. Fauci, “Polyangiitis overlap syndrome. Classification and prospective clinical experience,” American Journal of Medicine, vol. 81, no. 1, pp. 79–85, 1986. View at: Google Scholar
  20. C. W. Parker, “Allergic reactions in man,” Pharmacological Reviews, vol. 34, no. 1, pp. 85–104, 1982. View at: Google Scholar
  21. K.-R. Chen and J. A. Carlson, “Clinical approach to cutaneous vasculitis,” American Journal of Clinical Dermatology, vol. 9, no. 2, pp. 71–92, 2008. View at: Publisher Site | Google Scholar
  22. G. Sais, A. Vidaller, A. Jucgla, F. Gallardo, and J. Peyri, “Colchicine in the treatment of cutaneous leukocytoclastic vasculitis: results of a prospective, randomized controlled trial,” Archives of Dermatology, vol. 131, no. 12, pp. 1399–1402, 1995. View at: Publisher Site | Google Scholar
  23. R. K. Winkelmann, E. Wilson-Jones, N. P. Smith, J. S. C. English, and M. W. Greaves, “Neutrophilic urticaria,” Acta Dermato-Venereologica, vol. 68, no. 2, pp. 129–133, 1988. View at: Google Scholar
  24. W. Nurnberg, J. Grabbe, and B. M. Czarnetzki, “Urticarial vasculitis syndrome effectively treated with dapsone and pentoxifylline,” Acta Dermato-Venereologica, vol. 75, no. 1, pp. 54–56, 1995. View at: Google Scholar
  25. V. M. Martinez-Taboada, R. Blanco, M. Garcia-Fuentes, and V. Rodriguez-Valverde, “Clinical features and outcome of 95 patients with hypersensitivity vasculitis,” American Journal of Medicine, vol. 102, no. 2, pp. 186–191, 1997. View at: Publisher Site | Google Scholar
  26. J. C. Jennette, R. J. Falk, K. Andrassy et al., “Nomenclature of systemic vasculitides: proposal of an international consensus conference,” Arthritis and Rheumatism, vol. 37, no. 2, pp. 187–192, 1994. View at: Google Scholar
  27. G. A. Heresi and J. K. Stoller, “Augmentation therapy in α-1 antitrypsin deficiency,” Expert Opinion on Biological Therapy, vol. 8, no. 4, pp. 515–526, 2008. View at: Publisher Site | Google Scholar
  28. C. C. Te, V. Le, and M. Allee, “Famciclovir-induced leukocytoclastic vasculitis,” Annals of Pharmacotherapy, vol. 42, no. 9, pp. 1323–1326, 2008. View at: Publisher Site | Google Scholar
  29. R. Lin, “Unusual autoimmune manifestations in furosemide-associated hypersensitivity angiitis,” New York State Journal of Medicine, vol. 88, no. 8, pp. 439–440, 1988. View at: Google Scholar
  30. C. Bourgain, T. Bienvenu, A. C. Crémieux, A. Delage, and C. Carbon, “Bumetanide as replacement therapy in furosemide-induced vasculitis,” Presse Medicale, vol. 19, no. 32, pp. 1504–1505, 1990. View at: Google Scholar

Copyright © 2009 Nicola W. Mwirigi and Charles F. Thomas Jr. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

2864 Views | 450 Downloads | 0 Citations
 PDF  Download Citation  Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

We are committed to sharing findings related to COVID-19 as quickly and safely as possible. Any author submitting a COVID-19 paper should notify us at to ensure their research is fast-tracked and made available on a preprint server as soon as possible. We will be providing unlimited waivers of publication charges for accepted articles related to COVID-19. Sign up here as a reviewer to help fast-track new submissions.