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Erschienen in: Journal of Medical Case Reports 1/2015

Open Access 01.12.2015 | Case report

Pre-emptive steroids for a severe oedematous Buruli ulcer lesion: a case report

verfasst von: Daniel P O’Brien, Sarah Huffam

Erschienen in: Journal of Medical Case Reports | Ausgabe 1/2015

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Abstract

Introduction

Severe oedematous forms of Buruli ulcer (BU) often result in extensive tissue destruction, even with the institution of appropriate antibiotic treatment, leading to reconstructive surgery and long-term disability. We report a case of a patient with severe oedematous BU, which describes for the first time the pre-emptive use of prednisolone therapy commenced at the time of antibiotic initiation aimed at limiting the ongoing tissue destruction and its secondary sequelae.

Case presentation

A 91-year-old Australian-born Caucasian woman presented with a WHO category 3 oedematous BU lesion on the anterior aspect of her right ankle that she had first noticed three weeks earlier. Treatment was commenced with an antibiotic combination of rifampicin and ciprofloxacin. At the same time, pre-emptive prednisolone was commenced (a dose of 0.5mg/kg daily). Treatment resulted in rapid and significant reduction in the size of the induration associated with the lesion, and no significant increase in the size of the skin ulceration. Antibiotics were continued for 56 days and prednisolone therapy ceased 130 days after antibiotics commenced. No surgery was required. The wound healed completely after 10 months and there was no long-term limitation of movement at the ankle joint.

Conclusions

Pre-emptive corticosteroid therapy may prevent further progressive tissue necrosis and the need for secondary reconstructive surgery that commonly occurs during the antibiotic treatment of severe odematous forms of BU.
Hinweise

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

DOB and SH provided the clinical care to the patient and wrote the manuscript. Both authors read and approved the final manuscript.

Introduction

Mycobacterium ulcerans causes destructive lesions of skin and subcutaneous tissue known as Buruli ulcers (BU). They are found in 33 countries worldwide but most commonly in west and central Africa and south-eastern Australia. Oedematous cases are the most severe form of disease, and often result in extensive tissue destruction leading to reconstructive surgery and long-term disability [1,2]. Combination antimicrobial therapy is now recommended as first-line treatment of BU [3,4] and results in high cure rates, limiting the requirements for surgery [5,6]. However, with oedematous lesions ongoing tissue destruction and increasing ulceration generally occurs despite the administration of appropriate antibiotics and limits the success of early antibiotics [1,7].
We report a case of a patient with severe oedematous BU and describe for the first time the pre-emptive use of prednisolone therapy commenced with the initiation of antibiotic treatment that appeared to limit ongoing tissue destruction and of the need for reconstructive surgery.

Case presentation

A 91-year-old previously healthy Australian-born Caucasian woman living in a BU endemic area in Victoria, Australia, presented with a three-week history of a painful lesion on the anterior aspect of her right ankle. On examination she had an indurated, oedematous lesion of 210 × 120mm in diameter with central necrosis of 20 × 10mm diameter, classified as a WHO category 3 lesion (Figure 1). She weighed 52kgs, and had an estimated glomerular filtration rate of approximately 60mLs/minute. A diagnosis of an oedematous BU lesion was made based on the clinical appearance of the lesion and a positive M. ulcerans PCR of a swab of the lesion.
She was commenced on rifampicin 450mg daily and ciprofloxacin 500mg twice daily. As we were concerned she was at risk of further tissue necrosis, pre-emptive prednisolone of 30mg daily (0.5mg/kg/day) was initiated at the same time.
After three days the induration associated with the lesion had reduced by 74% to 120 × 55mm in diameter and the size of the ulceration remained stable (Figure 2, Table 1). Further reduction in induration had occurred by day 6 (Figure 3) and after four weeks of prednisolone combined with antibiotics there was no induration associated with the lesion and the size of the ulceration remained stable (Figure 4).
Table 1
Measurement of the area of skin induration and ulceration associated with the Buruli ulcer lesion according to the duration of treatment and dose of prednisolone
Days post start of treatment
Total induration (mm)
Total ulceration (mm)
Prednisolone dose (mg daily)
0
210 × 120
20 × 10
30
3
120 × 55
20 × 10
30
6
75 × 40
20 × 11
30
10
55 × 30
20 × 14
20
26
No additional induration
20 × 18
10
31
No additional induration
20 × 15
10
38
No additional induration
20 × 16
5
44
NR
NR
Cease
58
No additional induration
17 × 11
0
83
60 × 60
17 × 11
5
102
No additional induration
20 × 10
5
109
NR
NR
2.5
116
No additional induration
20 × 10
2.5
130
No additional induration
19 × 12
Cease
NR, not reviewed.
The ciprofloxacin dose was reduced at day 3 to 250 mg twice daily because of nausea potentially caused by relatively high systemic ciprofloxacin levels related to her advanced age and moderately reduced renal function, and after 26 days of antibiotics she developed a rash and the ciprofloxacin was replaced by clarithromycin 250mg twice daily. Antibiotics were ceased after a total of 56 days. The prednisolone was well tolerated and was initially weaned off over 44 days. However, due to a subsequent increase in induration associated with the lesion, it was recommenced at a low dose (5mg daily) 83 days after antibiotics commenced, then weaned off 130 days after antibiotics commenced (Table 1). No surgical debridement or reconstruction was required.
The lesion healed to a dry scab six months after commencing antibiotics, and had completely healed by 10 months (Figure 5). There was no permanent disability or limitation of movement at the ankle joint. There was no recurrence 12 months after treatment commenced.

Discussion

Oedematous lesions account for about 7% of BU cases seen in the Bellarine Peninsula, South-Eastern Australia [1]. Compared to non-oedematous lesions they are more likely to occur in diabetics and those who have a lesion on the hand, elbow or ankle [1]. They represent the most aggressive form of BU with 76% of lesions in our health service presenting at an advanced stage (WHO category 2 or 3) due to rapid progression and delays in diagnosis [1]. As a result, oedematous BU lesions are often associated with significant tissue necrosis, and this can progress even after the commencement of appropriate antibiotic treatment [1,7]. Severe lesions usually require debridement and reconstructive surgery (94% in our experience) [1], increasing the cost of treatment [8] and often resulting in long-term disability [9].
Reasons for the ongoing ulceration despite appropriate antibiotic treatment are not known but may include tissue swelling and secondary ischaemia of skin and superficial tissues resulting from paradoxical reactions, analogous to the paradoxical enlargement and suppuration of tuberculous lymphadenitis on treatment [10]. These commonly occur during or after the antibiotic treatment of BU lesions [5,11], and are more frequent in the treatment of oedematous forms of the disease [1]. Alternatively, it may be due to a delayed effect of persisting mycolactone, a potent exotoxin produced by M. ulcerans that is toxic to tissues [12]. We have previously reported successful use of prednisolone to limit tissue damage in patients experiencing severe BU-associated paradoxical reactions without negative effects on curative outcomes [13,14]. Research from the mouse model also suggests corticosteroids could potentially be utilised in the treatment of paradoxical reactions without reducing the effectiveness of antibiotic treatment [15]. Therefore, if paradoxical reactions are the cause of ongoing tissue loss in oedematous BU lesions on antibiotic treatment, we have previously postulated that pre-emptive prednisolone may prevent it [1].
In this case, at the time of commencing antibiotic treatment, we started pre-emptive prednisolone at the dose recommended for treatment of BU-associated paradoxical reactions [3]. The aim was to try and minimize the progression of tissue necrosis, the need for reconstructive surgery and long-term potential complications such as limitation of movement of the ankle joint, which would likely have occurred in the absence of pre-emptive treatment.
We postulate that the pre-emptive prednisolone treatment was effective in achieving these aims with no progression of the ulceration on treatment, a rapid reduction in the size of the associated induration, the avoidance of surgery and the lesion healing completely with no long-term sequelae such as limitation of movement at the ankle joint. Prednisolone was well tolerated in this patient. However, it can have potential adverse effects that need to be considered before use such as the potential to worsen co-existent infections including hepatitis B, tuberculosis and strongyloides (of particular concern in west and central Africa where most BU cases occur), destabilise diabetes, cause gastrointestinal ulceration, and progression of osteoporosis. Therefore, we believe that further study, including prospective trials, be performed to assess the safety and efficacy of pre-emptive corticosteroid therapy in patients with severe oedematous BU.
In this case, we used the initial antibiotic combination rifampicin and ciprofloxacin, which we have found to be highly effective in curing BU lesions and preventing disease recurrences [6,16-18]. However, it should be noted that although this combination is one of the recommended first-line antibiotic regimens for BU treatment by Australian experts, WHO recommends the use of rifampicin and streptomycin as the standard antibiotic regimen [4].

Conclusions

Our case suggests that pre-emptive corticosteroid therapy commenced at the time of antibiotic treatment initiation may prevent further progressive tissue necrosis and the need for secondary reconstructive surgery that commonly occurs during the antibiotic treatment of severe oedematous forms of BU.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Acknowledgements

We have no acknowledgements to report. There are no sources of funding to declare.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made.
The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
The Creative Commons Public Domain Dedication waiver (https://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

DOB and SH provided the clinical care to the patient and wrote the manuscript. Both authors read and approved the final manuscript.

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Metadaten
Titel
Pre-emptive steroids for a severe oedematous Buruli ulcer lesion: a case report
verfasst von
Daniel P O’Brien
Sarah Huffam
Publikationsdatum
01.12.2015
Verlag
BioMed Central
Erschienen in
Journal of Medical Case Reports / Ausgabe 1/2015
Elektronische ISSN: 1752-1947
DOI
https://doi.org/10.1186/s13256-015-0584-x

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