Cavitary pulmonary tuberculosis (TB) is extremely rare in infancy. Cavitation in lung in an infant usually suggests the diagnosis of staphylococcal pneumonia or congenital anomaly. Here we are reporting a 7 month, BCG vaccinated infant who presented with high-grade fever and cavitation on the chest x-ray. Reverse contact tracing did not reveal TB in parents or close relatives. We established the diagnosis of tuberculosis by demonstrating acid-fast bacilli in his gastric aspirate by smear and culture. We suggest that even in absence of suggestive history of TB, early morning gastric aspirate should be examined in all cases of non-resolving cavities in infants.
Cavitary lung diseases in infants are usually due to infections particularly by staphylococcus species or due to developmental abnormalities such as pulmonary vascular anomaly, congenital diaphragmatic hernia, pulmonary sequestrations etc. Cavities in tuberculosis (TB) usually occur in post-primary and sometimes in progressive primary TB which are rare in infancy and early childhood[1,2]. Only few cases of cavitary TB are reported from pediatric centres in India[1,3]. We are reporting a case of cavitary pulmonary tuberculosis in a 7-month old infant.
A 7-month old baby boy was brought to hospital with intermittent high grade fever and cough for past 2 months. There was no clinical improvement despite treatment with intravenous antibiotics including amoxicillin-clavulinic acid(100 mg/kg/day in divided doses for 7 days), ceftriaxone (100 mg/kg/day in divided in two doses for 7 days), linezolid (30 mg/kg/day in divided doses for 2 weeks), vancomycin (60 mg/kg/day in 4 divided doses for 7 days) and meropenem (60 mg/kg/day in divided doses for 5 days)by local pediatricians. Child had normal vaginal delivery with uneventful pre-natal period and birth weight was 2.85 kg. The child had received all vaccines as per National Immunisation Schedule including BCG. Examination revealed the baby was malnourished with weight (5 kg), length (55 cm) and both were below 3rd percentile of normal according to World Health Organisation (WHO) standard.The child was tachypneic (respiratory rate was 35/minute) and febrile (1020F). There was no significant lymphadenopathy or organomegaly. Examination of the respiratory system revealed intercostal retractions, bilateral crepitations and high pitched bronchial breath sound over left infraclavicular area. His peripheral blood showed haemoglobin 8.7 g/dl, total leukocyte count 12000/mm3 with neutrophils 50%, lymphocytes 47% and eosinophil 3%. His chest x-ray showed presence of a large cavity in the left upper zone, consolidation in the left lower zone and non-homogenous opacity in the right upper zone [Figure1]. Ultrasonography (USG) of whole abdomen was normal. High -resolution computed tomography (HRCT) of thorax revealed patchy consolidations in both lung fields and a large cavity in the left upper lobe [Figure2]. We aspirated his first morning gastric content through a paediatric Ryle’s tube and sent the sample for acid-fast bacilli (AFB) smear and mycobacterial BACTEC culture. Tubercle bacilli were identified under fluorescent microscopy. reveal any abnormality. We started category 1anti-tubercular therapy drugs (ATT) with daily isoniazid 50mg, rifampicin 50mg, pyrazinamide 125 mg, ethambutol 75mg for 2 months and isoniazid 50mg, rifampicin 50mg for last 4 months month. Fever subsided after 7 days of ATT and we discharged the child after 10 days in stable condition. Subsequently report of mycobacterial BACTEC culture came as positive and showed growth of Mycobacterium tuberculosis. At follow up after 8 weeks of ATT therapy, the child was doing well, asymptomatic and had radiological improvement of follow-up chest x-ray [Figure 3].
Infants, unlike adults, frequently present with unusual manifestations of TB and the diagnosis of TB is delayed or even missed. Cavity due to pulmonary tuberculosis in infancy is extremely rare but may occur as a consequence of progressive pulmonary TB in infancy which is believed to be a result of poor host defence responsible for multiplication of tubercle bacilli. Ultimately primary focus progresses to form area of consolidation. Later, the caseous areas in the lesion liquefies by proteolytic enzymes liberated from dead neutrophils and the liquid material discharges into bronchus forming cavity, known as primary cavitating tuberculosis (PCT) [1,4]. The incidence of PCT is now increasing in African and Indian children than children of western countries[1,4,5]. Early tuberculization, malnutrition and measles are the postulated causes of the epidemiological differences[1]. In a series of 75 cases of children younger than 2 years of age, Maniar et al. described five cases of cavitary TB in infants younger than 3 months of age with the youngest being 45 days [1].As per literature, BCG vaccination lowers the risk of progressive primary tuberculosis [6,7].Therefore BCG vaccination reduces the risk of PCT also. We excluded congenital TB as the baby did not fulfill the criteria (appearance of lesion in the first week of life, primary hepatic complex or caseating hepatic granuloma,
TB infection of placenta or the maternal genital tract and exclusion of possibility of post-natal transmission) proposed by Cantwell et al for the diagnosis of congenital TB[8]. Maternal genital TB was also excluded by gynaecological examination and USG whole abdomen of mother. Staphylococcal infection was ruled out on the basis of absence of response to anti-staphylococcal antibiotics and negative blood culture. HIV sero-negativity and localisation of infection in the form of cavity formation ruled out immune-compromisation in our case. Our case is unique as PCT by itself is an extremely rare entity in infancy. Moreover, absence of extra-pulmonary TB lesions, absence of history of contact with active TB cases and history of BCG vaccination made the diagnosis of PCT difficult.
Even in absence of history of contact, typical radiological pattern, extra-pulmonary involvement and positive tuberculin test clinicians should not rule out TB as a possibility and should perform early morning gastric lavage to confirm or to rule out TB in all non-resolving pneumonias during infancy.