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Raveendran MN, Srinivasan SM. Postpartum bullous pemphigoid – A case report. Our Dermatol Online. 2017;8(2):160-163.. |
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Postpartum bullous pemphigoid – A case report
Malar Nisha Raveendran, Sundaramoorthy M. Srinivasan
Department of Dermatology and STD, Chettinad Hospitals and Research Institute, Kelambakkam, Tamil Nadu, India
Corresponding author: Prof. Sundaramoorthy M. Srinivasan, E-mail: hamsrini@yahoo.co.in
Submission: 09.08.2016; Acceptance: 17.12.2016
DOI: 10.7241/ourd.20172.43
ABSTRACT
Bullous pemphigoid (BP) is an acquired autoimmune blistering disease occurring in the elderly more than 70 years of age though may occur during young age and childhood. BP is categorized by the development of urticarial plaques surmounted by sub epidermal blisters, and the deposition of immunoglobulin and complement at the basement membrane zone (BMZ) of the skin. BP is associated with other diseases, such as diabetes mellitus, thyroid disorders, rheumatoid arthritis and malignancies. Heat shock proteins (HSP) are a family of proteins that are produced by cells in response to exposure to stressful conditions. Heat shock protein 90 (HSP90) inhibitors potentially target for the autoimmune disease and chronic inflammatory diseases. We present a case of 21 year old lactating female, a known case of hyperthyroidism with an abrupt onset of fluid filled vesicles and bullae over the abdomen and limbs since 3 days associated with itching. She had similar episodes before and was diagnosed and treated for BP. She had a flare up of the disease due to the personal stress in the patient as Heat shock proteins plays an important role in the pathophysiology of BP. Following treatment upon continuous follow ups, there were no flare up of the disease. Here in this patient, apart from hypothyroidism, stress also acts as a trigger in BP.
Key words: Bullous pemphigoid; Pregnancy; Heat shock proteins; Immune modulation
INTRODUCTION
Bullous pemphigoid (BP) is an acquired autoimmune blistering disorder occurring in the elderly individuals more than 70 years of age [1]. It is also reported in young age and during infancy and childhood [2]. The incidence in people older than 80 years is 150-180 per million per year [1]. BP is the most common bullous disease in Western Europe than in India [2].
Heat shock proteins (HSP) are a family of proteins that are produced by cells in response to exposure to stressful conditions. They were first described in relation to heat shock [3]. Hence the name. But are now known to also be expressed during other stresses including exposure to cold [4], UV light [5], and during wound healing or tissue remodelling. The heat shock proteins are also referred to as stress proteins and their up regulation is sometimes described more generally as part of the stress response [6].
CASE REPORT
A 21 year old lactating female, married since one year presented to us with an abrupt onset of fluid filled vesicles and bulla over the abdomen and limbs since 3 days associated with itching with few erosions. She presented with history suggestive of wheal formation and severe itching prior to the development of lesions. No history of spontaneous rupture of lesions, peripheral extension, mucosal lesions or history suggestive of healing with milia formation. No history of prior drug intake, or any constitutional symptoms, systemic involvement in the patient. Patient gave history of personal stress following her delivery. She’s a known case of hypothyroidism and is on continuous treatment with T. Eltroxin 25mcg for 4 years. Two years back, patient had similar episodes following stressful events and was on treatment with systemic corticosteroids. No flare up of the disease was seen in these two years. Elective LSCS done on 23-09-2015, delivered a healthy girl baby weighing 2.5 kg.
Cutaneous examination revealed multiple tense vesicles and bullae with clear filled fluid over an erythematous base predominantly over the flexural aspects of upper limb, medial aspects of thighs and few over the trunk and abdomen interspersed with few erosions and crusting (Figs. 1 and 2). Oral cavity and genital examination were normal. Nikolsky’s sign was negative and Bullae spreading sign was positive. Elsewhere the skin was normal. Her baby was healthy and did not show any skin lesions. A differential diagnosis of bullous pemphigoid was considered.
Laboratory investigations were done; complete blood analysis revealed an eosinophil count of 9.8%. Histopathological investigation of a fresh intact bullae showed sub epidermal cleft with mixed infiltrate of eosinophils and neutrophils (Fig. 3). Based on the clinical and histopathology finding a diagnosis of BP was confirmed.
Pediatrician advice was sought regarding the baby’s condition which was normal and suggested to continue breast feeding as steroids are under category B which will not be harmful to the baby. General physician advised to continue T. Eltroxin 25mcg for the patient’s hypothyroid status.
Patient was treated with oral prednisolone 1mg per kg body weight, to which she had a dramatic response. Patient improved symptomatically and was discharged after two weeks. She has been under regular follow up for past 8 months and asymptomatic till now.
DISCUSSION
BP is an increasingly common immunobullous disease of the elderly, and, due to the late age of onset, is rarely seen in women of fertile age [7]. Mucous membrane involvement may be seen in 10%-30% of patients [2]. The term BP was coined by Lever in 1953 [8]. Women and men are equally afflicted.
The etiology of BP is idiopathic. Genetic susceptibility shows a strong association with HLA-DQB1*0301 [9]. Precipitating factors include influenza vaccination, UV light, radiotherapy for breast cancer, thermal and electric burns, percutaneous endoscopic gastrostomy, amputation stump, incisional hernia scar, and injection or an adhesive dressing [10]. Certain infections like cytomegalovirus, Ebstein-Barr virus, HHV-6, HHV-8, hepatitis B and C viruses, Helicobacter Pylori and Toxoplasma Gondii [2,9] and certain drugs like furosemide, enalapril, phenacitin, ibuprofen, sulfa pyridine also induces BP [10]. Stress also plays as a trigger in the manifestation of BP [11].
The pathogenesis of BP is characterized by tissue-bound and circulating IgG autoantibodies against two components of the hemi desmosome of stratified epithelia, BP 230 kD (BPAg1) and BP 180 kD (BPAg2) [2]. BP manifests as tense blisters on urticarial base more commonly in the lower abdomen, thighs and forearms although they may occur anywhere. Pruritus is present and may be persist for several months. The blister ruptures to leave erosions which heal rapidly with post inflammatory hyperpigmentation.
Histopathology shows sub epidermal clefts and dermal inflammatory infiltrate composed predominantly of eosinophil and neutrophils [1].
BP is associated with other diseases, such as diabetes mellitus, thyroid disorders, rheumatoid arthritis, pemphigus foliaceus, dermatomyositis, ulcerative colitis, multiple autoimmune diseases, myasthenia gravis and malignancies [10]. As per the 2012 BAD guidelines, both systemic and topical corticosteroids and anti-inflammatory antibiotics are given for mild and moderate cases. In cases of severity, steroid sparing agents like azathioprine, methotrexate, dapsone, MMF and chlorambucil are given [12].
In 2001 Gee BC et al described BP in two patients that have differed in the disease behaviour during pregnancy [7]. This patient had her first episode 2 years before pregnancy, she was totally asymptomatic during pregnancy, now the patient had a flare up 3 months after pregnancy.
Heat-shock proteins are named according to their molecular weight [13]. Heat shock protein 90 (HSP90) is involved in conformational and structural maturation of signalling molecules and transcription factors in immune reaction. HSP90 inhibitors induce immune modulation via anti-inflammatory effect, regulating humoral and cellular immune responses. Therefore, HSP90 inhibitors potentially useful target for the autoimmune disease and chronic inflammatory diseases. In 2015, studies performed by Stephan Tukaj et al provide an important insight that Hsp90 were highly expressed in the epidermis of BP patients, but its serum levels were decreased and inversely associated with autoantibodies against BP180 NC16A. It may be speculated that anti-BP180 NC16A autoantibodies indirectly lead to an enhanced intracellular expression of Hsp90 by generation of an inflammatory response comprising soluble pro-inflammatory mediators (cytokines and ROS) and simultaneously cause a direct inhibition of its cellular release [14,15].
In the above discussed case, patient had her first episode 2 years before pregnancy due to the stressful events, she was totally asymptomatic during pregnancy, now the patient had a flare up 3 months after pregnancy. She gave a history of personal stress after delivery following which she developed a flare up of the disease. Due to the stress and hypothyroidism in this patient, she developed BP during the postpartum and not during pregnancy because of the maintained guarded therapy during her initial episode. Upon follow up visits, there were no flare up of the disease as the stress reduced and the thyroid levels were maintained.
CONCLUSION
BP is the most common autoimmune blistering disorder occurring in the elderly individuals more than 70 years of age. As per the literature, BP among young people is more severe and more active than the usual form in the elderly. Autoantibodies to stress proteins like Hsp90 also plays an important role in the pathogenesis of BP.
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Notes
Source of Support: Nil
Conflict of Interest: None declared.
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