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PREGNANCY IN A PATIENT OF HANSEN’S DISEASE

Ashok Kumar Shukla, Asha Dalal

 
Hensen’s disease is a chronic granulomatous disease caused by infection with mycobacterium leprae. Mrs. SAK 25 yrs old married housewife primigravida with 6 months amenorrhoea was referred from peripheral hospital in view of well defined, erythematous lesions on her hands. No further signs of leprosy in the skin, the mucosae and the peripheral nerves were found. Fite-Faraco staining of the skin biopsy showed sporadic acid - fast bacilli and con.rmed an active tuberculoid leprosy. Outpatient treatment was immediately initiated with oral rifampicin 600 mg monthly and Dapsone 100 mg daily.

However the patient went in labour at 35 wks period of gestation and delivered vaginally on 15.7.2002 male child 2.1 kgs cried immediately after birth Apgar 8,9,9.

INTRODUCTION

Hensen’s disease is a chronic granulomatous disease caused by infection and mycobacterium leprae. The exact
mechanism of transmission of M. Lepra remains unknown. The hallmark clinical .ndings in leprosy are hypopigmented skin lesions with loss of sensation. Depending upon the number of lesions and the number of bacillus observed on lesion’s smear.

CASE REPORT
Mrs. SAK 25 yrs old married housewife primigravida with six months amenorrhoea was referred from peripheral hospital
in view of well defined, erythematous lesions on her hands. No specific past signi.cant history. On examination: her vitals were in normal limits, On local examination: well defined, elevated erythematous lesions on her hands with central anaesthesia in the lesions. On per abdomen examination : Uterus was 24 wks size, variable presentation, foetal movements present, foetal heart sound present. No further signs of leprosy in the skin, the mucosae and the peripheral nerves were found. Fite-Faraco staining of the skin biopsy showed sporadic acid-fast bacilli and con.rmed an active tuberculoid leprosy. Out patient treatment was immediately initiated with oral rifampicin 600 mg monthly and Dapsone 100 mg daily. During the treatment cycle the skin lesions vanished.

Additional leprosy reactions did not occur and the medication was well tolerated. However the patient went in labour at
35 wks period of gestation and delivered vaginally on 15.7.2002 male child 2.1 kg cried immediately after birth Apgar 8,9,9. On 5th postnatal day mother and baby were discharged and advised to follow up on OPD basis.

DISCUSSION
Leprosy can be classified in 3 groups: 1) Borderline leprosy (2) Paucibacillary or Tuberculoid leprosy (3) Multibacillary or Lepromatous leprosy. Skin biopsy and smears are helpful in establishing the diagnosis of leprosy. Pregnancy in women with leprosy is a hazardous undertaking.1 The pregnant state causes a relative decrease in cellular immunity. This decrease allows Mycobacterium leprae to pro.lerate, which may precipitate or worsen disease, leading to permanent nerve damage.2 Careful management of reactional states and treatment of patients with dapsone monotherapy can prevent this nerve damage. Infants are usually much less affected than mothers; however, selection of the mother’s antimicrobial regimen must ensure adequate control of the bacteria while avoiding teratogenicity and in utero adverse effects.1,2 Dapsone is the only drug which is comparatively safe in pregnancy. Because of thalidomide’s potential for causing serious birth defects it's again contraindicated in pregnancy. Various studies have concluded that leprosy in pregnancy can be treated safely and successfully by combined drug therapy.3 Pregnancy is a trigger factor for reaction. Up to 20% of children born to mothers with leprosy may develop leprosy by puberty. Increased awareness and health education, as well as long term surveillance of ‘cured’ leprosy patients, are essential to break a potentially vicious cycle of leprosy and pregnancy.1
REFERENCES
1. Duncan ME. An historical and clinical review of the interaction of leprosy and pregnancy : a cycle to be broken.
Soc Sci Med 1993; 37 (4) : 457-72.
2. Lyde CB. Pregnancy in patients with Hansen disease. Arch
3.. Dermatol 1997; 133 (5) : 623-7.
3. Neuer A, Spang E, Stitcht-Groh V. Initial manifestation of tuberculoid leprosy in pregnancy. Guidelines for diagnosis and therapy. Geburtshilfe Frauenheilkd 1996; 56 (3) : 156-60.
1. Duncan ME. An historical and clinical review of the interaction of leprosy and pregnancy : a cycle to be broken.
Soc Sci Med 1993; 37 (4) : 457-72.
2. Lyde CB. Pregnancy in patients with Hansen disease. Arch
3.. Dermatol 1997; 133 (5) : 623-7.
3. Neuer A, Spang E, Stitcht-Groh V. Initial manifestation of tuberculoid leprosy in pregnancy. Guidelines for diagnosis and therapy. Geburtshilfe Frauenheilkd 1996; 56 (3) : 156-60.

MASSAGE TREATMENT FOR BACK PAIN
Evidence for symptomatic relief is encoruaging but not compelling
Swedish massage is a touch therapy that uses a range of techniques to manipulate the soft tissues of the body : effleurage (slow rhythmic stroking), kneading (circular compression), petrissage (forceful skin rolling, friction (penetrating pressure from the .ngertips with circular or transverse movement), tapotement (percussive movements), vibration (trembling movement of both hands). In most English speaking countries, massage is seen as an alternative or complementary treatment.

Most massage therapists are convinced that massage treatment is free of risk. This is not true. Too much force can cause fractures of osteoporotic bones; and even rupture of the liver and damage to nerves have been associated with massage. These events are rarities and massage is relatively safe, provided that well trained therapists observe the contraindications.
BMJ, 2003; 326 : 562.

TREATMENT OF ANCA ASSOCIATED VASCULITIS
The rate of relapse was similar among patients receiving maintenance immunosuppressive treatment with azathioprine and among those receiving maintenance treatment with cyclophosphamide.

Early substitution of azathioprine for cyclophosphamide can reduce the rate of toxic effects associated with long-term cyclophosphamide treatment of autoantibodies to neutrophil cytoplasmic antigens (ANCA)-Associated vasculitis.

N Engl J Med, 2003; 349 : 36.



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