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2.
J Gastroenterol Hepatol ; 33(12): 1969-1974, 2018 Dec.
Article in English | MEDLINE | ID: mdl-29845642

ABSTRACT

BACKGROUND AND AIMS: Vulval Crohn's disease (VCD) is a rare extra-intestinal cutaneous manifestation of Crohn's disease. VCD is often unrecognized and misdiagnosed and can be difficult to treat. The aim of the study was to describe the clinical presentation, associated features, and response to treatment modalities in patients with VCD. METHODS: A prospective review of patients with VCD who were referred to our specialist dermatology clinic from 2003 to 2017 was performed. Data on age at diagnosis, presenting signs, associated features, and response to treatment were collected. RESULTS: Thirty-one patients with a median age of 40 years (range 13-66 years) were identified. VCD manifested most frequently with vulval edema (77%), ulceration (35%), and fissures (39%). Eighty-one percent had active gastrointestinal disease. Oral involvement and pyoderma gangrenosum were present in 13% and 19%, respectively. Topical therapy was effective in mild VCD. Tumor necrosis factor-α inhibitors were the most effective second-line therapy, with 53% achieving complete clinical remission. Additionally, we have found compression garments and shorts to be useful adjuncts in treating vulval edema. CONCLUSIONS: Vulval Crohn's disease is a diagnostic and therapeutic challenge. We recommend consideration of tumor necrosis factor-α inhibitors at an early stage.


Subject(s)
Crohn Disease/complications , Edema/etiology , Skin Ulcer/etiology , Vulvar Diseases/etiology , Adolescent , Adult , Aged , Anti-Inflammatory Agents/administration & dosage , Biological Products/administration & dosage , Biopsy , Compression Bandages , Crohn Disease/diagnosis , Crohn Disease/immunology , Crohn Disease/therapy , Edema/diagnosis , Edema/immunology , Edema/therapy , Female , Humans , Middle Aged , Prospective Studies , Remission Induction , Skin Ulcer/diagnosis , Skin Ulcer/immunology , Skin Ulcer/therapy , Time Factors , Treatment Outcome , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Tumor Necrosis Factor-alpha/immunology , Vulvar Diseases/diagnosis , Vulvar Diseases/immunology , Vulvar Diseases/therapy , Young Adult
5.
Article in English | MEDLINE | ID: mdl-25549312

ABSTRACT

PURPOSE: To assess the efficacy of Botulinum toxin A (BoNT-A) in the treatment of patients with hypercontractile stomas resulting in repeated pouching system failures and leaks. DESIGN: Prospective case series. SUBJECTS AND SETTING: Ten consecutive patients who presented to the outpatient stoma clinic with actively contractile stomas that shortened spasmodically resulting in leaks were offered treatment with BoNT-A if treatment with other measures had been unsuccessful. METHODS: Following an observed reduction in the peristalsic shortening of a stoma after intradermal injection of BoNT-A for hyperhidrosis, we conducted a prospective case series of 10 patients with pouch adhesive failures attributed to spasmodic shortening of the stoma. Ten patients, 3 with urostomies and 7 with ileostomies, were offered BoNT-A injection. The first was treated cautiously with 15 units of BoNT-A injected into the muscularis layer, followed by an additional 25 units injected 1 month later. Subsequent patients received doses varying from 50 to 100 units. Ongoing treatments ranged 50 to 100 units every 3 to 6 months. RESULTS: Seventy percent (n = 7) of patients reported a useful reduction in leakage and pouching system seal failures. In these 7 patients, the frequency of pouch changes changed from an average of 2.18 to 0.44 per day (over all 10 patients this was a change from an average of 2.35 per day to 1.16 per day). No adverse side effects were reported. CONCLUSION: Findings from this clinical case series suggest that BoNT-A may be a promising treatment in the management of patients with leaks caused by actively contracting stomas.


Subject(s)
Botulinum Toxins, Type A/drug effects , Botulinum Toxins, Type A/therapeutic use , Ileostomy/nursing , Neuromuscular Agents/therapeutic use , Surgical Stomas/adverse effects , Botulinum Toxins, Type A/adverse effects , Humans , Injections, Intradermal , Neuromuscular Agents/pharmacology , Treatment Outcome
6.
BMJ Case Rep ; 20142014 Dec 22.
Article in English | MEDLINE | ID: mdl-25535230

ABSTRACT

A 75-year-old man with ulcerative colitis (UC) and diet controlled diabetes mellitus presented with a 3-week history of slightly itchy, red plaques on both lower limbs ascending gradually to cover the trunk and arms. One week later, he developed a flare up of his UC. Routine blood tests showed modest drop in haemoglobin (122 g/L) and C reactive protein (85 mg/L). Serology was remarkable for high antiproteinase 3 (c-ANCA). Serum electrophoresis showed a mildly positive paraprotein band (γ region). Stool culture was negative. Urine analysis showed proteinuria. Skin biopsy showed features of urticarial vasculitis (UV). He underwent a flexible sigmoidoscopy after the flare up showed mildly active UC. The patient was given hydrocortisone for 7 days and then prednisolone. Both rash and UC subsided. Electrophoresis was repeated 4 weeks later showing normal pattern. Prednisolone has been gradually reduced. Although rare, UV can be considered as one of the skin manifestations of UC.


Subject(s)
Colitis, Ulcerative/complications , Skin/pathology , Urticaria/etiology , Vasculitis/etiology , Aged , Anti-Inflammatory Agents/therapeutic use , Antibodies, Antineutrophil Cytoplasmic/blood , Colitis, Ulcerative/blood , Colitis, Ulcerative/pathology , Humans , Hydrocortisone/therapeutic use , Male , Prednisolone/therapeutic use , Urticaria/diagnosis , Urticaria/drug therapy , Vasculitis/diagnosis , Vasculitis/drug therapy , Vasculitis, Leukocytoclastic, Cutaneous/diagnosis , Vasculitis, Leukocytoclastic, Cutaneous/drug therapy , Vasculitis, Leukocytoclastic, Cutaneous/etiology
7.
Dermatol Ther (Heidelb) ; 4(2): 271-9, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25005352

ABSTRACT

BACKGROUND: Stomal leaks can be associated with significant social, psychological and physical morbidity for ostomy patients. Poor fitting of the stoma appliance due to irregularities of skin contours is one cause of stoma leaks which commonly result in secondary irritant dermatitis prompting presentation to a dermatologist. In addition to skin-directed topical therapy and review of stoma appliances, correction of contour defects with intradermal injections of filler materials is one possible treatment to improve adhesion and reduce leaks. CASES: We report eight cases of ostomy patients, who presented with stoma leaks and associated dermatitis, who were treated with intradermal injections of the porcine collagen (Permacol™) or subcutaneous injections of polyacrylamide hydrogel (Aquamid Reconstruction™) for correction of skin contour defects. Resolution or improvement of symptoms was achieved for five patients, and no complications were noted as a result of treatment. CONCLUSIONS: This report represents the largest series of ostomy patients treated for correction of peristomal skin contour defects with injection therapy. Treatment was well tolerated and performed in the outpatient setting under local anesthetic. Attempted correction of peristomal skin contour defects using injection of filler materials represents a potential alternative to surgical intervention and can result in significant benefits for the patient.

8.
Dermatol Ther (Heidelb) ; 4(1): 137-40, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24496772

ABSTRACT

INTRODUCTION: Inflammatory bowel disease has been associated with a number of cutaneous and systemic neutrophilic disorders, including pyoderma gangrenosum. In 1972, the term chronic multi-focal recurrent osteomyelitis was given to a sterile neutrophilic condition which has been associated with inflammatory bowel disease. CASE REPORT: We report a case of a 23-year-old man with long-standing severe Crohn's disease which necessitated subtotal colectomy. He subsequently developed progressive, intermittent back pain that were limiting his functional movement. Numerous investigations to identify what initially was thought to be an infectious process failed to lead to the diagnosis. Biopsy of the spine identified a sterile neutrophilic infiltrate and the diagnosis of chronic recurrent multi-focal osteomyelitis was made which was successfully treated with immunosuppressive drugs. CONCLUSION: Inflammatory bowel disease can present with cutaneous and systemic neutrophilic disorders and this association is becoming increasingly recognized by gastroenterologists and dermatologists. Chronic recurrent multi-focal osteomyelitis is a sterile neutrophilic disorder which can present with bone pain and responds to immunosuppressive therapy.

9.
Orbit ; 33(2): 129-31, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24410585

ABSTRACT

Pyoderma gangrenosum is a rare condition with few cases of eyelid involvement reported in the literature. Pathergy is a well-recognised phenomenon that can trigger this condition. Pyoderma gangrenosum should be considered in cases of progressive cribriform cicatrisation where there is a history of antecedent trauma. Surgical management of a resultant ectropion may be challenging as a result of aggressive scarring and the risk of provoking a recurrence. We report a case of pyoderma gangrenosum causing a cicatricial ectropion, and discuss the underlying aetiology of iatrogenic incitement, and its implications for surgical management.


Subject(s)
Cicatrix/therapy , Cyclosporine/therapeutic use , Ectropion/therapy , Immunosuppressive Agents/therapeutic use , Pyoderma Gangrenosum/complications , Skin Transplantation , Cicatrix/etiology , Combined Modality Therapy , Ectropion/etiology , Humans , Male , Middle Aged
10.
Dermatol Ther (Heidelb) ; 3(2): 199-202, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24318417

ABSTRACT

Vulval involvement in Crohn's disease (CD) is rare, particularly in children. The clinical features include erythema, edema, ulceration, and labial skin tags. The authors present two cases of children with vulval CD. In both cases, marked labial edema was the presenting feature. In one patient the immunomodulator tacrolimus ointment 0.03% was used with success. In the second patient control was achieved with intralesional triamcinolone in combination with systemic metronidazole.

11.
Dermatol Ther (Heidelb) ; 3(2): 211-4, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24281763

ABSTRACT

Ciclosporin is widely used in a number of inflammatory disorders and has the potential for drug interactions. We report here a case of acute kidney injury due to the interaction of ciclosporin with methyl-1-testosterone. This has not been previously reported and it is relevant as methyl-1-testosterone can be purchased online. Physicians should be aware of any over the counter or online purchased "supplements" and consider possible drug interactions.

13.
Ostomy Wound Manage ; 58(12): 34-8, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23221017

ABSTRACT

Bullous pemphigoid (BP) is a blistering disorder of the skin and mucosa that may coexist with inflammatory bowel disease (IBD). The authors' experiences with peristomal and generalized BP in five patients (three with ulcerative colitis [UC] post colostomy surgery and two with Crohn's disease [CD] post ileostomy surgery, time since surgery 5 to 20 years) is described. The patients presented with peristomal blisters and erosions, subsequently confirmed as BP by skin biopsy. Treatments for the skin disease included potent alcohol-based topical corticosteroids, oral tetracyclines, and oral corticosteroids. In three patients (two with UC, one with CD), the initially localized peristomal disease later became generalized across the skin; these patients were more likely to require systemic immunosuppressive therapy. Because an involvement of plectin, a cytoskeletal protein that attaches skin and mucosal cells to their extracellular matrix, in IBD has been shown, it is possible that this protein forms the missing link between IBD and BP via epitope spreading. The inflammation of IBD exposes plectin, stimulating a secondary immune response that may, in susceptible individuals, crossreact with the skin, provoking BP. Further research into this area could enable clinical testing for plectin auto-antibodies in patient sera, possibly preempting the development of BP and expediting the initiation of early effective treatment.


Subject(s)
Inflammatory Bowel Diseases/complications , Pemphigoid, Bullous/complications , Plectin/physiology , Aged , Aged, 80 and over , Female , Humans , Inflammatory Bowel Diseases/physiopathology , Male , Middle Aged , Pemphigoid, Bullous/physiopathology
19.
Ostomy Wound Manage ; 56(1): 45-7, 2010 Jan 01.
Article in English | MEDLINE | ID: mdl-20093717

ABSTRACT

Primary adenocarcinoma at an ileostomy site is an exceedingly rare occurrence but has been documented at the peristomal skin of patients with a long-standing ileostomy. Chronic irritation and resultant metaplasia is thought to be a key underlying mechanism for this phenomenon. Biopsy of newly developing lesions in the peristomal area of long-standing stomas is essential in order to avoid delayed diagnosis and limit complications. A 37-year-old man with a history of ulcerative colitis and ileostomy surgery 18 years prior presented with an asymptomatic polypoid lesion at the mucocutaneous junction. Initially diagnosed as pyogenic pranuloma, the lesion was treated using topical silver nitrate. This did not resolve the lesion but ulceration and bleeding were observed. A biopsy showed evidence of primary adenocarcinoma arising from the ileostomy site. The lesion was removed surgically, an ileo-anal J pouch was created, and the patient is currently receiving long-term follow-up and monitoring for any possible future complications. This case study is one of several in the literature suggesting that a high index of suspicion is warranted when ileostomy patients, especially those with a history of ulcerative colitis, present with unusual peristomal lesions.


Subject(s)
Adenocarcinoma/complications , Colitis, Ulcerative/surgery , Ileostomy/adverse effects , Skin Neoplasms/complications , Adult , Humans , Male
20.
Pediatr Dermatol ; 26(6): 730-4, 2009.
Article in English | MEDLINE | ID: mdl-20199451

ABSTRACT

We describe two cases of PHACES syndrome that illustrate the importance of recognizing this rare syndrome. As children with this syndrome can present to general pediatricians, dermatologists, pediatric cardiologists, ophthalmologists, and neurologists, it is important that all are aware of the spectrum of associated abnormalities.


Subject(s)
Abnormalities, Multiple/pathology , Aortic Coarctation/pathology , Cranial Fossa, Posterior/abnormalities , Eye Abnormalities/pathology , Hemangioma/pathology , Astigmatism/pathology , Child , Disease Progression , Female , Humans , Infant , Magnetic Resonance Imaging , Male , Prognosis
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