Parvovirus B19-associated hydrops fetalis: the first confirmed case in Hong Kong

ABSTRACT

Hong Kong Med J 1998;4:321-3 | Number 3, September 1998
CASE REPORT
Parvovirus B19-associated hydrops fetalis: the first confirmed case in Hong Kong
PKS Chan, KF To, SK Yip, JSL Tam, AFB Cheng
Department of Microbiology, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong
 
 
We describe a case of asymptomatic human parvovirus B19 infection during pregnancy that led to hydrops fetalis and foetal death. The diagnosis was confirmed by the presence of parvovirus B19-specific IgM antibodies in the maternal serum and the pathognomonic findings, which showed intranuclear eosinophilic viral inclusions and margination of chromatin in foetal cells of haemopoietic lineage. Details of clinical, virological, and histological findings are presented. Difficulties in confirming the diagnosis of parvovirus B19 infection in Hong Kong are discussed.
 
Key words: Fetal death/etiology; Hydrops fetalis/etiology; Parvoviridae/immunology; Parvovirus B19, human; Pregnancy complications, infections/microbiology
 
View this abstract indexed in MEDLINE:
 

Acute Wernicke's encephalopathy complicating chronic gallstone ileus

ABSTRACT

Hong Kong Med J 1998;4:235-8 | Number 2, June 1998
CASE REPORT
Acute Wernicke's encephalopathy complicating chronic gallstone ileus
WF Ng, CS Ng
Department of Pathology, Yan Chai Hospital, 7-11 Yan Chai Street, Tsuen Wan, Hong Kong
 
 
An autopsy performed on a 53-year-old man who had unrelieved obstruction of the small bowel due to gallstone ileus revealed morphological features that were typical of acute Wernicke's encephalopathy. The likely sequence of disease in this patient was the development of thiamine deficiency owing to the unrelieved intestinal obstruction, which resulted in the development of acute Wernicke's encephalopathy. A high clinical awareness is required for the diagnosis of acute Wernicke's encephalopathy in patients with malnutrition from any cause.
 
Key words: Acute disease; Intestinal obstruction; Wernicke's encephalopathy/diagnosis; Wernicke's encephalopathy/etiology; Wernicke's encephalopathy/pathology; Thiamine deficiency
 
View this abstract indexed in MEDLINE:
 

Primary hyperparathyroidism in Hong Kong: an analysis of 44 cases

ABSTRACT

Hong Kong Med J 1998;4:229-34 | Number 2, June 1998
CASE REPORT
Primary hyperparathyroidism in Hong Kong: an analysis of 44 cases
FKW Chan, SC Tiu, KL Choi, TK Au Yong, LF Tang
Department of Medicine, Queen Elizabeth Hospital, 30 Gascoigne Road, Kowloon, Hong Kong
 
 
Primary hyperparathyroidism is increasingly being diagnosed subsequent to the detection of hypercalcaemia using multichannel auto-analyser screening. This paper provides a local picture of the clinical presentation and management of primary hyperparathyroidism. A retrospective review was conducted of 44 patients with primary hyperparathyroidism who were treated at the Queen Elizabeth Hospital between January 1987 and July 1996. Twenty-five (56.8%) of the patients were asymptomatic. Only three (6.8%) patients gave radiograms that had features indicating primary hyperparathyroidism; seven (15.9%) had renal stones. The patients underwent one or more of the following localisation procedures: computerised tomography, ultrasonography, thallium-technetium subtraction scanning, and technetium Tc 99m sestamibi scanning. The latter method was the most sensitive (64.3%). Ten adenomas that could not be localised by any of these procedures were successfully removed during surgery. Surgery was successful in 94.4% of cases and surgical outcome was comparable to that reported in the literature.
 
Key words: Hyperthyroidism/complications; Hyperthyroidism/diagnosis; Hyperthyroidism/therapy; Parathyroid neoplasms/pathology; Parathyroid neoplasms/radiography; Parathyroid neoplasms/radionuclide imaging; Parathyroid neoplasms/surgery; Technetium Tc 99m sestamibi/diagnostic use
 
View this abstract indexed in MEDLINE:
 

A case of eosinophilic gastroenteritis

ABSTRACT

Hong Kong Med J 1998;4:226-8 | Number 2, June 1998
CASE REPORT
A case of eosinophilic gastroenteritis
YQ Hsu, CYF Lo
Room 218A, Tung Ying Building, 100 Nathan Road, Kowloon, Hong Kong
 
 
Eosinophilic gastroenteritis is a rare disorder characterised by eosinophilic infiltration of the bowel wall and various gastrointestinal manifestations. Diagnosis requires a high index of suspicion and exclusion of various disorders that are associated with peripheral eosinophilia. We report on a woman who had a short history of abdominal pain and ascites, and who responded dramatically to a course of low-dose steroid.
 
Key words: Ascites/pathology; Eosinophilia/diagnosis; Eosinophils; Food hypersensitivity/complications; Gastroenteritis/therapy
 
View this abstract indexed in MEDLINE:
 

Treatment of vitiligo with autologous epidermal transplantation using the roofs of suction blisters

ABSTRACT

Hong Kong Med J 1998;4:219-24 | Number 2, June 1998
CASE REPORT
Treatment of vitiligo with autologous epidermal transplantation using the roofs of suction blisters
WYM Tang, LY Chan, KK Lo
Social Hygiene Service, Department of Health, Social Hygiene Clinic, 3/F Lek Yuen Health Centre, Shatin, Hong Kong
 
 
We report our experience of autologous epidermal transplantation for three patients with vitiligo. The vitiligo in two patients was stable whereas that in the third was active. Autologous epidermal transplantation using suction blister roofs from normally pigmented skin was performed following the failure to repigment skin using topical steroid and/or psoralen-ultraviolet A treatment. Grafts were well taken in all three patients. Satisfactory repigmentation was noted in the two patients who had stable vitiligo; there were no complications except for mild hyperpigmentation at the donor areas. For the patient who had active vitiligo, depigmentation of the graft and concomitant Koebner's phenomenon at the donor site were observed 3 weeks after the procedure. We conclude that autologous epidermal transplantation using the roofs of suction blisters is an excellent and safe repigmenting procedure for stable, localised vitiligo and that active disease precludes transplantation.
 
Key words: Epidermis/surgery; Vitiligo/therapy; Transplantation, autologous
 
View this abstract indexed in MEDLINE:
 

A case of colonic tuberculosis mimicking Crohn's disease

ABSTRACT

Hong Kong Med J 1998;4:63-6 | Number 1, March 1998
CASE REPORT
A case of colonic tuberculosis mimicking Crohn's disease
CF Lau, AMC Wong, KS Yee, CK Loo, PK Hui, KM Lam
Department of Medicine, Kwong Wah Hospital, 25 Waterloo Road, Kowloon, Hong Kong
 
 
A 26-year-old Thai woman who has lived in Hong Kong for the past 3 years presented with a 2-month history of feverishness, intermittent epigastric discomfort, anorexia, and weight loss. She had had per rectal bleeding for 10 days. Colonoscopy on two separate occasions revealed multiple ulcerations involving the entire colon, with rectal sparing. Histological examination of the two sets of colonic biopsies that were obtained during colonoscopy suggested Crohn's disease. There was no response to mesalazine and metronidazole, but the patient responded promptly to a therapeutic trial of antituberculous drugs. Cultures from the first set of colonic biopsies were negative for acid-fast bacilli, but 8 weeks after the second colonoscopy, cultures from the second set of biopsies yielded Mycobacterium tuberculosis. This case illustrates that the diagnosis of colonic tuberculosis requires a high index of suspicion. In cases where the information available does not reveal a definite differentiation between colonic tuberculosis and Crohn's disease, corticosteroids should be withheld. The administration of corticosteroids to a patient with colonic tuberculosis may have disastrous results, and a therapeutic trial of antituberculous drugs should be considered instead.
 
Key words: Crohn disease; Diagnosis, differential; Mycobacterium tuberculosis; Tuberculosis, gastrointestinal
 
View this abstract indexed in MEDLINE:
 

Penicillium marneffei infection and solitary pulmonary nodule

ABSTRACT

Hong Kong Med J 1998;4:59-62 | Number 1, March 1998
CASE REPORT
Penicillium marneffei infection and solitary pulmonary nodule
KC Chang, CK Chan, KC Chow, CW Lam
Department of Respiratory Medicine, Ruttonjee Hospital, 266 Queen's Road East, Hong Kong
 
 
We report on a patient infected with human immunodeficiency virus who presented with fever, a solitary pulmonary nodule, and cervical lymphadenopathy. The diagnosis of Penicillium marneffei infection was made from an excisional lymph node biopsy and a sputum culture. The microbiology, pathology, diagnosis, and treatment of the case are discussed. A high level of clinical suspicion is necessary for making an early diagnosis and improving the outcome of infection.
 
Key words: AIDS-related opportunistic infections; Antifungal agents; Coin lesion, pulmonary; HIV infections/complications; Penicillium
 
View this abstract indexed in MEDLINE:
 

Streptococcal toxic shock-like syndrome in a post-myomectomy patient

ABSTRACT

Hong Kong Med J 1998;4:52-6 | Number 1, March 1998
CASE REPORT
Streptococcal toxic shock-like syndrome in a post-myomectomy patient
SM Choo, SW Yeo, E Thomas
Department of Anaesthesia, Kandang Kerbau Women's and Children's Hospital, 100 Bukit Timah Road, Singapore 229899
 
 
We report on a healthy 34-year-old woman who received an elective myomectomy for uterine fibroid, and postoperatively developed fatal streptococcal toxic shock-like syndrome. We discuss the series of events that led to this life-threatening disease and its pathophysiology, and suggest areas in which management might have been improved.
 
Key words: Fatal outcome; Postoperative complications; Shock, septic; Streptococcus pyogenes
 
View this abstract indexed in MEDLINE:
 

Creutzfeldt-Jakob disease in Hong Kong

ABSTRACT

Hong Kong Med J 1997;3:439-43 | Number 4, December 1997
CASE REPORT
Creutzfeldt-Jakob disease in Hong Kong
KKP Ng, PCK Li, CK Wong, JHM Chan, JHM Yeung, KT Loo
Department of Medicine, Queen Elizabeth Hospital, Kowloon, Hong Kong
 
 
Two elderly patients presented with rapidly progressive dementia and their electroencephalograms showed periodic discharges. Creutzfeldt-Jakob disease was pathologically confirmed in one of the patients. Striking clinical features and characteristic electroencephalograms should prompt the clinical diagnosis in most patients.
 
Key words: Creutzfeldt-Jakob syndrome; Dementia; Electroencephalography; Encephalopathy, bovine spongiform; Prion diseases
 
View this abstract indexed in MEDLINE:
 

Hereditary angioedema in a Chinese family

ABSTRACT

Hong Kong Med J 1997;3:436-8 | Number 4, December 1997
CASE REPORT
Hereditary angioedema in a Chinese family
D Choy, A Ho, JKW Chan, CKW Lai, E Li, R Leung
Department of Medicine, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong
 
 
Hereditary angioedema is characterised by recurrent episodes of peri-orbital and peri-oral swelling which can cause an upper airway obstruction, abdominal pain, vomiting, diarrhoea, and even hypotensive collapse. This potentially fatal condition is frequently misdiagnosed; its early recognition and appropriate treatment are thus important. We report a familial cluster of hereditary angioedema in a Chinese family and describe the clinical course of two patients.
 
Key words: Angioneurotic edema; Complement 1 inactivators; Immunologic deficiency syndromes
 
View this abstract indexed in MEDLINE:
 

Pages