Article Information

Kyoung Sook Park MD, PhD^1#, Seungtaek Lee^3#, Jeong Hae Kie MD², Ea Wha Kang MD, PhD^1*

^#Authors contributed equally

¹Division of Nephrology, Department of Internal Medicine, Gyeonggi-do, South Korea

²Department of Pathology, NHIS Ilsan Hospital, Gyeonggi-do, South Korea

³Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea

^*Corresponding Author: Dr. Ea Wha Kang, Division of Nephrology, Department of Internal Medicine, NHIS Ilsan Hospital, 100 Ilsan-ro, Ilsan-donggu, Goyang, Gyeonggi-do 10444, Republic of Korea

Received: 15 March 2020; Accepted: 26 March 2020; Published: 05 May 2020

Citation: Kyoung Sook Park, Seungtaek Lee, Jeong Hae Kie, Ea Wha Kang. A Case Report of Phenytoin-Induced Anti-Neutrophil Cytoplasmic Antibody (ANCA) Associated Vasculitis. Archives of Clinical and Medical Case Reports 4 (2020): 356-361.

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Abstract

Keywords

Phenytoin; Drug; Vasculitis; ANCA-associated vasculitis

Article Details

Abbreviations:

ANCA: anti-neutrophil cytoplasmic antibody; UPCR: urine protein to creatinine ratio; UACR: urine albumin-creatinine ratio; Anti-MPO antibody: anti-myeloperoxidase antibody; IV: intravenous

1. Introduction

After discovery of the anti-neutrophil cytoplasmic antibody (ANCA), certain drugs were revealed to cause drug-induced ANCA-associated vasculitis [1-4]. Proper diagnosis of drug-induced vasculitis is very important to prevent fatal clinical outcomes by ceasing the causative drug [3, 4]. Phenytoin is a widely used anticonvulsant, but it has been sporadically mentioned throughout previous decades as a rare causative drug of ANCA-associated vasculitis, which is often fatal [5-7]. Therefore, we report a case of phenytoin-induced ANCA-associated vasculitis to arouse awareness.

2. Case Report

A 65-year-old male patient was transferred to the emergency room with alteration of a semi-coma mental status and seizure due to intracerebral hemorrhage. The patient had an unremarkable medical history. Phenytoin (300 mg/day) was administered for the anti-epileptic effect, but it was discontinued after one month of administration due to newly developed agranulocytosis. Ten days later, the patient had complaints of generalized edema and purpura on both legs. Laboratory tests showed acute glomerulonephritis with a serum creatinine concentration of 2.36 mg/dL, and urinalysis indicated proteinuria (2+) and hematuria (3+; red blood cell count >20/HPF). The spot urine protein to creatinine ratio (UPCR) was 10,938.4 mg/g, and the spot urine albumin-creatinine ratio (UACR) was 5,500 mg/g. Antinuclear antibody testing showed a positive result with a speckled pattern (titer 1:80), and testing for atypical pattern ANCA (p-ANCA, anti-myeloperoxidase (MPO) antibody) also showed a positive result with the titer of 12.0 index in the enzyme-linked immunosorbent assay. Serum complement level was normal, and all viral serology tests showed negative results. The kidney biopsy was performed, and on histologic examination, two out of six glomeruli showed cellular crescent with fibrinoid necrosis. Compared with glomerular change, the interstitial inflammation was active and severe, and the infiltrating inflammatory cells were polymorphous, including many numbers of neutrophils and eosinophils, with lymphocytes, plasma cells, and histiocytes. Focal ill-defined granuloma was observed in the interstitium, and there was no specific immunofluorescent activity. On electron microscopy, the foot processes were focally effaced, but there was no electron dense deposit. With ANCA-positive serologic findings, the diagnosis of necrotizing glomerulonephritis, mixed type, was completed. Based on the histological finding in the interstitium, additional comments on the possibility of drug-induced ANCA-associated vasculitis were described (Figure 1). However, we could not determine any suspected drug at the time of pathologic diagnosis.

The patient was treated with high-dose methylprednisolone intravenous (IV) for three days and then oral prednisolone (1 mg/kg/day), followed by IV cyclophosphamide (500 mg/m²). Moreover, the patient underwent hemodialysis to control intractable pulmonary edema and uremic symptoms. The renal function was gradually recovered, and serum creatinine decreased to 1.43 mg/dL. After nine days of immunosuppressive treatment, the patient had another seizure, and thus was re-treated with phenytoin. Ten days after phenytoin re-administration, pancytopenia was developed again, and serum creatinine increased to 1.99 mg/dL. Because of the aggravation of renal dysfunction after re-administration of phenytoin and the pathologic suspicion of drug-induced ANCA-associated vasculitis, phenytoin was suspected as the causative agent. Phenytoin therapy was stopped. After discontinuation of phenytoin, pancytopenia was recovered, and serum creatinine levels decreased to 1.29 mg/dL. The titer of p-ANCA decreased to within the reference range (Figure 2). The cyclophosphamide therapy was discontinued, and prednisolone dose was gradually tapered and discontinued after two months.

Discussion and Conclusions

This is a case report of a 65-old male patient with phenytoin-induced ANCA-associated vasculitis who responded well to discontinuation of phenytoin and treatment with an immunosuppressant. Drug-induced vasculitis is an uncommon type of vasculitis seen in clinical practice [4, 8]. On one hand, increasing numbers of new drugs on the market, especially biological agents, have become new causative agents associated with drug-induced vasculitis [4]. Among them, phenytoin-associated vasculitis is very rare, but its prognosis is too serious to disregard [5, 6]. In two case series with a total of 13 patients from over 20 years ago, only three patients limited to manifestations on the skin with steroids survived, but all of the rest showed mortality [5, 6]. Histologic findings revealed severe diffuse granulomatous vasculitis or fibrinoid necrosis of the vascular walls with eosinophilic infiltrate in the aforementioned case series, which has close similarity with our case. Unlike primary ANCA-associated vasculitis, drug-induced ANCA-associated vasculitis is characterized by the following; a) serum ANCA test was positive, of which the immuno-staining pattern is atypical because of its multi-antigenicity, such as mixed cytoplasmic and perinuclear fluorescence, which can be explained by the fact that ANCA is directed to one or more neutrophil cytoplasm antigens, including MPO, human leukocyte elastase, cathepsin G, and lactoferrin, and b) clinical course is temporally related to the administration of any causative drugs [8]. Clinical presentation can vary from nonspecific symptoms, such as myalgia, arthralgia and skin rash, to severe symptoms, such as multiple organ damage. The kidney is the most commonly involved organ with proteinuria, hematuria, and renal function deterioration [3, 4].

Recent advances in epigenetics, genetic predispositions, and neutrophil extracellular traps are providing new insights into the pathogenesis and identification of susceptible individuals to drug-induced vasculitis [4]. Because withdrawal of the offending agent is the primary intervention, interest and knowledge about drug-induced vasculitis are of utmost importance for earlier diagnosis and prevention of severe organ damage. In this case, we could not suspect phenytoin as the causative agent at the initial presentation although atypical p-ANCA immunostaining pattern and histologic findings suggested the possibility of drug-induced vasculitis. We were able to suspect the relation between phenytoin and vasculitis by chasing the clinical course, which declined after phenytoin re-administration. We also could confirm the connection through improvement of the patient’s clinical course following discontinuation of phenytoin treatment. This emphasizes that a high index of suspicion, careful drug history, and awareness about potential causative drugs are essential to diagnose drug-induced vasculitis earlier. There are no standard treatment guidelines for drug-induced ANCA-associated vasculitis, but steroid and immunosuppressive treatment should be considered for vasculitis that has invaded major organs [3, 4]. In this case, discontinuing phenytoin, high-dose steroid, and cyclophosphamide therapy was effective for the patient.

Because systemic vasculitis induced by phenytoin rarely occurs, this serious side effect has only been sporadically case-reported, which was not well characterized as an entity of drug-induced vasculitis. Therefore, we would like to share this case to help physicians to be more conscious about phenytoin-induced vasculitis when they prescribe phenytoin as anti-epileptic treatment.

Acknowledgments

Not applicable.

Conflict of Interest

None.

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