Focal fatty change: a rare hepatic manifestation of diabetes mellitus

ABSTRACT

Hong Kong Med J 1996;2:99-101 | Number 1, March 1996
CASE REPORT
Focal fatty change: a rare hepatic manifestation of diabetes mellitus
WK Ng, IOL Ng
Department of Pathology, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong
 
 
Focal fatty change of the liver is a rare and poorly recognised entity. Most of the previously reported cases occurred in patients suffering from the usual steatogenic conditions, such as diabetes mellitus and obesity. The focality of the lesion, however, remains unexplained. The author reports a rare case of subcapsular focal fatty change of the liver occurring in a 60-year-old Chinese woman suffering from poorly controlled adult-onset diabetes mellitus. The underlying pathogenesis for the focal fatty change is thought to be related to local ischaemic effect secondary to diabetic angiopathy, which may further enhance the steatogenicity of diabetes mellitus. The recognition of focal fatty change of the liver is important in order to avoid misdiagnosis of other space-occupying lesions radiologically and macroscopically.
 
Key words: Fatty liver; Liver; Diabetes mellitus; Diabetes mellitus, adult-onset
 
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Cerebral atrophy in heroin abuse

ABSTRACT

Hong Kong Med J 1996;2:96-8 | Number 1, March 1996
CASE REPORT
Cerebral atrophy in heroin abuse
DTS Lee, AT Ahuja, KO Ng, C Chan, CM Leung, CN Chen
Substance Abuse Unit, Department of Psychiatry, The Chinese University of Hong Kong, Shatin, Hong Kong
 
 
Although psychoactive substance abuse has been known to cause cerebral atrophy, there are no previous reports of a similar nature pertaining to the use of heroin. We describe a 26-year-old male intravenous heroin abuser who had prominent cerebral atrophy that could not be explained by other medical conditions. The possible relationship between cerebral atrophy and chronic heroin use is discussed.
 
Key words: Substance abuse; Substance abuse, intravenous; Substance abuse, complications; Heroin dependence; Atrophy, cerebral
 
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Association of paralytic ileus, interstitial cystitis and hydronephrosis with systemic lupus erythematosus

ABSTRACT

Hong Kong Med J 1995;1:354-6 | Number 4, December 1995
CASE REPORT
Association of paralytic ileus, interstitial cystitis and hydronephrosis with systemic lupus erythematosus
TN Chau, ST Lai
Department of Medicine, Princess Margaret Hospital, Laichikok, Kowloon, Hong Kong
 
 
We report the case of a 25-year-old woman who presented with paralytic ileus, interstitial cystitis and bilateral hydronephrosis with systemic lupus erythematosus being the probable underlying aetiology. This uncommon association-the first case described in our locality-may represent a specific subgroup found in lupus patients.
 
Key words: Paralytic ileus; Interstitial cystitis; Systemic lupus erythematosus
 
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Reversible acute renal failure in a patient with IgA nephropathy

ABSTRACT

Hong Kong Med J 1995;1:351-3 | Number 4, December 1995
CASE REPORT
Reversible acute renal failure in a patient with IgA nephropathy
SL Lui, KW Chan, TM Chan, IKP Cheng
Division of Nephrology, Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong
 
 
Reversible acute renal failure is a rare complication of IgA nephropathy. We report a patient with IgA nephropathy who developed acute renal failure after an episode of gross haematuria. Renal biopsy revealed extensive acute tubular damage and red blood cell casts. His renal failure recovered spontaneously without specific treatment. The clinical and pathological features of this IgA nephropathy complication are discussed.
 
Key words: IgA nephropathy; Gross haematuria; Acute renal failure
 
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Magnetic resonance imaging: evaluation of recurrent eosinophilic granuloma of the ilium

ABSTRACT

Hong Kong Med J 1995;1:348-50 | Number 4, December 1995
CASE REPORT
Magnetic resonance imaging: evaluation of recurrent eosinophilic granuloma of the ilium
KS Tai, FL Chan, ACW Lee
Department of Diagnostic Radiology, Queen Mary Hospital, Pokfulam, Hong Kong
 
 
A case of eosinophilic granuloma of the ilium is reported, in which the patient was examined by magnetic resonance imaging for post-operative evaluation purposes. Magnetic resonance imaging, combined with contrast enhancement and fat suppression technique, is a sensitive way of detecting recurrent eosinophilic granuloma involving the bony skeleton.
 
Key words: Eosinophilic granuloma; Magnetic resonance imaging
 
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Rhabdomyolysis and heroin addiction

ABSTRACT

Hong Kong Med J 1995;1:266-8 | Number 3, September 1995
CASE REPORT
Rhabdomyolysis and heroin addiction
SH Wan, ML Szeto
Department of Medicine, Tuen Mun Hospital, Tuen Mun, Hong Kong
 
 
In recent years there has been an increased number of reports of rhabdomyolysis associated with heroin addiction and other drugs such as cocaine, amphetamines, salicylates, and alcohol. Early diagnosis and treatment can prevent serious complications such as acute renal failure. We describe a case of an intravenous heroin addict with rhabdomyolysis and acute renal failure which required acute haemodialysis. A high index of suspicion for rhabdomyolysis and myoglobinuria is essential in drug overdose patients when admitted to hospital. The prognosis for adequately treated cases of rhabdomyolysis is often excellent.
 
Key words: Rhabdomyolysis; Heroin; Creatine kinase; Diagnosis
 
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The use of fluorescence in situ hybridization in the diagnosis of a case of DiGeorge anomaly

ABSTRACT

Hong Kong Med J 1995;1:263-5 | Number 3, September 1995
CASE REPORT
The use of fluorescence in situ hybridization in the diagnosis of a case of DiGeorge anomaly
KM Tsui, YY Ng, WL Yu, TS Lam
Clinical Genetic Service, Department of Health, 2/F, Cheung Sha Wan Jockey Club Clinic, Sham Shui Po, Hong Kong
 
 
DiGeorge anomaly comprises hypoparathyroidism, thymic aplasia, conotruncal cardiac anomaly and dysmorphic features. Most cases result from a microdeletion within chromosome 22q11. We report a case of documented DiGeorge anomaly and the use of high resolution cytogenetic analysis and the fluorescence in situ hybridization technique are discussed.
 
Key words: DiGeorge Anomaly; In situ hybridization, fluorescence
 
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Spontaneous internal jugular vein thrombosis and metastic adenocarcinoma of unknown primary

ABSTRACT

Hong Kong Med J 1995;1:258-60 | Number 3, September 1995
CASE REPORT
Spontaneous internal jugular vein thrombosis and metastic adenocarcinoma of unknown primary
WM Lam, AT Ahuja, CO Mok, C Metreweli
Department of Diagnostic Radiology and Organ Imaging, Prince of Wales Hospital, Shatin, Hong Kong
 
 
Internal jugular vein thrombosis is difficult to diagnose clinically. Real time ultrasound should be the investigation of choice. For spontaneous jugular vein thrombosis associated with adenocarcinoma of unknown primary, further imaging to search for the primary tumour is probably not justified because of the poor prognosis of the patient.
 
Key words: Spontaneous internal jugular vein thrombosis; Real time ultrasound; Adenocarcinoma of unknown primary
 
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Fulminant idiopathic hypereosinophilic syndrome

ABSTRACT

Hong Kong Med J 1995;1:150-2 | Number 2, June 1995
CASE REPORT
Fulminant idiopathic hypereosinophilic syndrome
FH Ng, HL Kong, WF Ng, KY Lam, CC Chan, CM Chang
Department of Medicine, Ruttonjee Hospital, 266 Queen's Road East, Hong Kong
 
 
We report a patient with rapidly fatal idiopathic hypereosinophilic syndrome presenting with tetraparesis and acute congestive heart failure. Post-mortem examination showed extensive myocardial necrosis but no pathology in the brain. The possible mechanisms leading to organ damage and the treatment of this condition are discussed.
 
Key words: Eosinophilia; General paralysis; Congestive heart failure; Myocarditis
 
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Fibrillary glomerulonephritis: a case report

ABSTRACT

Hong Kong Med J 1995;1:69-71 | Number 1,March 1995
CASE REPORT
Fibrillary glomerulonephritis: a case report
SL Lui, KW Chan, FK Li, TM Chan, IKP Cheng
Division of Nephrology, Department of Medicine, Queen Mary Hospital, Pokfulam, Hong Kong
 
 
Fibrillary glomerulonephritis is a recently recognised condition. The usual presentation is heavy proteinuria. The diagnosis is established by demonstration of the characteristic Congo-red negative, randomly arranged microfibrils in the glomeruli by electron microscopy. At present, there is no proven effective treatment for this condition and the prognosis is generally poor. The first case of fibrillary glomerulonephritis diagnosed in Hong Kong is reported here in a 38-year-old woman.
 
Key words: Fibrillary; Glomerulonephritis; Nephrotic syndrome
 
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