A case of thoracic empyema due to suppurative melioidosis

ABSTRACT

Hong Kong Med J 2001;7:201-4 | Number 2, June 2001
CASE REPORT
A case of thoracic empyema due to suppurative melioidosis
TY Tsang, ST Lai
Department of Medicine, Princess Margaret Hospital, Princess Margaret Hospital Road, Laichikok, Kowloon, Hong Kong
 
 
Melioidosis is considered a rare disease in Hong Kong, and its diagnosis and treatment can be difficult. We report the case of a patient who presented with thoracic empyema. The material sampled from the empyema was initially labelled Burkholderia cepacia. The diagnosis of melioidosis due to Burkholderia pseudomallei could only be made after repeated cultures, and performing arginine dihydrolase and serological tests. The patient was initially treated with imipenem for 2 weeks, and then with ciprofloxacin as maintenance therapy. A resistant strain of the organism developed after 7 months of treatment. The patient was then given co-amoxiclav. Repeated courses of surgical drainage and debridement were also instituted. Subsequent computed tomographic scanning of the thorax showed gradual resolution of the empyema.
 
Key words: Burkholderia pseudomallei; Meliodosis; Pseudomonas pseudomallei; Suppurative meliodosis; Thoracic empyema
 
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Porphyria cutanea tarda and melioidosis

ABSTRACT

Hong Kong Med J 2001;7:197-200 | Number 2, June 2001
CASE REPORT
Porphyria cutanea tarda and melioidosis
WK Fung, SCF Tam, KM Ho, P Lam, KK Lo
Social Hygiene Service, Department of Health, 3/F Sai Ying Pun Polyclinic, 134 Queen's Road West, Hong Kong
 
 
Porphyria cutanea tarda is a metabolic disorder in the haem biosynthetic pathway. It includes a heterogeneous group of conditions, which may be inherited or, more commonly, acquired. Although porphyria cutanea tarda presents with cutaneous lesions only, it is often associated with systemic disease. A 64-year-old Chinese patient, who developed sporadic porphyria cutanea tarda 1 year after the diagnosis of pulmonary melioidosis, is discussed. The patient presented with a history of recurrent photosensitive vesicles, blisters, and skin fragility on the sun-exposed areas of both forearms and hands, 6 months after commencing doxycycline and amoxycillin. Both the histological and biochemical findings were characteristic of porphyria cutanea tarda. All the lesions subsided after cessation of these antibiotics. The patient was free of further lesions at follow-up 6 months later. The association seen in this case between porphyria cutanea tarda and melioidosis is unlikely to be coincidental, because these two diseases are both very rare in Hong Kong. In addition, the temporal relationship between the antibiotic therapy and the clinical course of skin lesions in this patient suggests that the drugs were a trigger factor, precipitating their appearance.
 
Key words: Adult; Antibiotic; Meliodosis; Porphyria cutanea tarda/diagnosi
 
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First fatal case of enterovirus 71 infection in Hong Kong

ABSTRACT

Hong Kong Med J 2001;7:193-6 | Number 2, June 2001
CASE REPORT
First fatal case of enterovirus 71 infection in Hong Kong
DKK Ng, AKW Law, SWW Cherk, KL Mak
Department of Paediatrics, Kwong Wah Hospital, Waterloo Road, Hong Kong
 
 
Enteroviruses are a common cause of childhood infections, from hand, foot and mouth disease, to lethal brainstem encephalitis. Enterovirus 71 was first isolated in 1969. Brainstem encephalomyelitis and pulmonary oedema are postulated to be causally related and have been found to be a common feature of fatal enterovirus 71 cases. A fatal case of enterovirus 71 infection in a 2-year-old, previously healthy boy is reported. He presented to the Department of Paediatrics with clinical features of sepsis within 3 days of onset of fever. A few minutes after injection of midazolam, fentanyl and vecuronium for intubation, cardiac arrest developed and was not amenable to various treatment modalities. Pulmonary haemorrhage and oedema were noted during intubation, and postmortem examination confirmed the presence of brainstem encephalomyelitis.
 
Key words: Child; Disease outbreaks; Enterovirus infections, epidemiology; Hand, foot and mouth disease
 
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Neuroleptic malignant syndrome induced by droperidol

ABSTRACT

Hong Kong Med J 2001;7:101-3 | Number 1, March 2001
CASE REPORT
Neuroleptic malignant syndrome induced by droperidol
PC So
Department of Anaesthesiology, North District Hospital, 9 Po Kin Road, Sheung Shui, New Territories, Hong Kong
 
 
A case of droperiodol-induced neuroleptic malignant syndrome during anaesthesia is presented. An 86-year-old male underwent spinal anaesthesia for open reduction and internal fixation of a trochanteric hip fracture. He received droperidol 5 mg intravenously for sedation towards the end of surgery. He subsequently became very drowsy and experienced marked muscle rigidity and autonomic instability. He became febrile postoperatively. The clinical syndrome resolved after 12 hours. When using droperidol in anaesthesia or intensive care--especially when large doses are given--the development of neuroleptic malignant syndrome should be suspected if the patient becomes febrile and has muscle rigidity and autonomic instability.
 
Key words: Antipsychotic agents/adverse effects; droperidol/adverse effects; Neuroleptic malignant syndrome
 
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Surgery for intractable epilepsy in a 14-year-old girl

ABSTRACT

Hong Kong Med J 2001;7:97-100 | Number 1, March 2001
CASE REPORT
Surgery for intractable epilepsy in a 14-year-old girl
WW Cheng, H Otsubo, OC Snead
Department of Paediatrics, Caritas Medical Centre, 111 Wing Hong Street, Shamshuipo, Hong Kong
 
 
We report on a 14-year-old girl who presented with a 2-year history of simple and complex partial seizures with secondary generalisation. Monotherapy using carbamazepine and combination therapy using carbamazepine and gabapentin had been tried within the 2 years before presentation. Seizure control, however, was poor. Magnetic resonance imaging showed structural abnormalities over the right occipital and temporal lobes. Continuous scalp video electroencephalography was performed over 4 days, during which six clinical seizures were associated with electroencephalography changes at the right occipital and temporal lobes. Invasive intracranial video electroencephalography identified a focus at the right occipital lobe, a focus at the right temporal lobe that spread rapidly to the right parietal lobe, and an irritative zone over the posterior part of the right frontal lobe. Functional mapping delineated the motor and sensory cortices. Right temporal lobectomy, right occipitoparietal cortical excision, and multiple subpial transections of the posterior part of the right frontal lobe were performed. For 16 months after the surgery, the patient has been seizure-free while receiving drug treatment, and the only complication reported has been a segmental loss of the left visual field.
 
Key words: Brain diseases/surgery; Child; Electroencephalography; Epilepsy, temporal lobe/surgery; Magnetic resonance imaging
 
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Classic late infantile neuronal ceroid lipofuscinosis in a Chinese patient

ABSTRACT

Hong Kong Med J 2001;7:93-6 | Number 1, March 2001
CASE REPORT
Classic late infantile neuronal ceroid lipofuscinosis in a Chinese patient
CH Ko, CK Kong, TC Chow, KC Lee
Department of Paediatrics, Caritas Medical Centre, 111 Wing Hong Street, Shamshuipo, Hong Kong
 
 
Neuronal ceroid lipofuscinoses are a group of rare neurodegenerative disorders that are characterised by an accumulation of autofluorescent lipopigments in neurons and extraneuronal tissues. We report on a 4-year-old boy who presented with an acute onset of seizures followed by rapid psychomotor deterioration, ataxia, and visual failure. Photic stimulation at 1 to 3 Hz elicited discrete spike and wave discharges in the electroencephalogram, which were diminished at a higher frequency of stimulation. The electroretinogram was extinct. Magnetic resonance imaging of the brain showed generalised cerebral and cerebellar atrophy. Electron microscopic examination of lymphocytes and samples of muscle and skin revealed characteristic curvilinear inclusion bodies. To our knowledge, this is the first case of late infantile neuronal ceroid lipofuscinosis to be reported in a Hong Kong Chinese patient.
 
Key words: Child, preschool; Convulsions/etiology; Electroencephalography; Magnetic resonance imaging; Neuronal ceroid-lipofuscinosis
 
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Meningoencephalitis caused by Bacillus cereus in a neonate

ABSTRACT

Hong Kong Med J 2001;7:89-92 | Number 1, March 2001
CASE REPORT
Meningoencephalitis caused by Bacillus cereus in a neonate
WP Chu, TL Que, WK Lee, SN Wong
Department of Paediatrics, Tuen Mun Hospital, Tsing Chung Koon Road, Tuen Mun, New Territories, Hong Kong
 
 
We report on a newborn boy, who was delivered at 26 weeks' gestation by emergency caesarean section because of a prolapsed cord and breech presentation. Grade IV hyaline membrane disease subsequently developed, for which a surfactant was given. On day 8, there were frequent apnoeic attacks, and on day 30, marked irritability developed, as did intermittent stiffening of all four limbs. The anterior fontanelle was bulging and tense, and the cerebrospinal fluid was found to be turbid. Gram staining of the cerebrospinal fluid and blood revealed Gram-positive bacilli. Subsequent culturing yielded Bacillus cereus, which was sensitive to amikacin and vancomycin. Severe cerebral oedema developed, however, and computed tomography of the brain showed bright cortical sulci, suggestive of meningitis. The baby died on day 37, and post-mortem histological examination of the brain showed extensive liquefactive necrosis with abundant neutrophilic infiltration. Since infection with Bacillus cereus is rapidly fatal, early recognition of infection by this organism is important.
 
Key words: Bacillus cereus; Bacillaceae infections; Brain/pathology; Infant, newborn; Meningoencephalitis
 
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Crusted (Norwegian) scabies in two old-age home residents

ABSTRACT

Hong Kong Med J 2000;6:428-30 | Number 4, December 2000
CASE REPORT
Crusted (Norwegian) scabies in two old-age home residents
LY Chan, WYM Tang, HHF Ho, KK Lo
Social Hygiene Service, Department of Health, Hong Kong
 
 
Scabies is commonly seen in hospitals, where it frequently affects geriatric and convalescent patients. The clinical features of the classic form of scabies are well recognised. Crusted (Norwegian) scabies, which is a hyperinfestation variant of scabies, is very contagious and can present as other dermatoses, thus delaying the correct diagnosis and management. Two residents of different old-age homes presented with hyperkeratotic skin eruptions, which later proved to be crusted scabies. In both cases, the scabies was initially misdiagnosed as eczema. The delay in making a correct diagnosis led to an outbreak of scabies in the old-age home in which one of the patients was residing.
 
Key words: Aged; Scabes/pathology; Sarcoptes scabiei; Skin/parasitology
 
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Abdominal pregnancy presenting as a missed abortion at 16 weeks' gestation

ABSTRACT

Hong Kong Med J 2000;6:425-7 | Number 4, December 2000
CASE REPORT
Abdominal pregnancy presenting as a missed abortion at 16 weeks' gestation
KY Kun, PY Wong, MW Ho, CM Tai, TK Ng
Department of Obstetrics and Gynaecology, Pamela Youde Nethersole Eastern Hospital, 3 Lok Man Road, Chai Wan, Hong Kong
 
 
We report on an abdominal pregnancy that presented as a missed abortion at 16 weeks' gestation and review the literature on the management of abdominal pregnancy. The clinical presentation of abdominal pregnancy varies, and the diagnosis depends on a high index of suspicion. Ultrasonography is useful for early diagnosis of the condition. The management depends on the gestation at presentation; for advanced abdominal pregnancy, surgical intervention is recommended. The treatment of the placenta is a matter of controversy. In general, expectant management is suggested. When the placenta is left behind, the use of prophylactic methrotrexate is not advocated. An awareness of abdominal pregnancy is very important for reducing associated morbidity and mortality.
 
Key words: Laparotomy; Pregnancy, abdominal/ultrasonography; Pregnancy complications; Pregnancy outcome
 
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Hypothyroidism presenting as hypercholesterolaemia and simvastatin-induced myositis

ABSTRACT

Hong Kong Med J 2000;6:423-4 | Number 4, December 2000
CASE REPORT
Hypothyroidism presenting as hypercholesterolaemia and simvastatin-induced myositis
YT Hung, VTF Yeung
Department of Medicine and Geriatrics, Our Lady of Maryknoll Hospital, 118 Shatin Pass Road, Wongtaisin, Hong Kong
 
 
We report on a 50-year-old woman who presented with hypertension. She was given simvastatin for hypercholesterolaemia. The creatine kinase level was 3180 U/L at the 3-month follow-up visit, which was thought to be due to simvastatin treatment. Although treatment was discontinued, the creatine kinase level 4 months later remained higher than 3000 U/L. Echocardiography revealed mild pericardial effusion and normal left ventricular function; the electromyogram was also normal. The patient subsequently showed signs and symptoms suggestive of hypothyroidism, which was confirmed by measurements of the concentration of thyroid-stimulating hormone (>100 mU/L) and free thyroxine (<2 pmol/L). Thyroxine replacement therapy normalised the creatine kinase and cholesterol levels. This case illustrates the importance of excluding underlying causes of hypercholesterolaemia before contemplating lipid-lowering therapy.
 
Key words: Hypercholesterolemia; Hypertension/complications; Hypothyroidism; Lipids/blood; Myositis/chemically induced
 
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