Twists and turns in the body: an imaging spectrum

ABSTRACT

Hong Kong Med J 2010;16:390-6 | Number 5, October 2010
MEDICAL PRACTICE
Twists and turns in the body: an imaging spectrum
Shiobhon Y Luk, KH Fung
Department of Radiology, Pamela Youde Nethersole Eastern Hospital, Chai Wan, Hong Kong
 
 
Life is full of twists and turns. These surprises can sometimes be wonderfully invigorating. Twists and turns can also occur in the body, however, sometimes with dangerous consequences. Torsion and volvulus are important causes of acute abdominal pain. The clinical symptoms and signs associated with torsion and volvulus are often non-specific and are difficult to diagnose clinically. Clinicians frequently rely on imaging methods to make the diagnosis. Prompt and accurate diagnosis is important to avoid the life-threatening complications of torsion and volvulus. Therefore, it is helpful to be familiar with the features of torsion and volvulus.
 
Key words: Diagnostic imaging; Intestinal volvulus; Stomach volvulus; Torsion abnormality; Uterine diseases
 
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Diagnostic challenges of human brucellosis in Hong Kong: a case series in two regional hospitals

ABSTRACT

Hong Kong Med J 2010;16:299-303 | Number 4, August 2010
MEDICAL PRACTICE
Diagnostic challenges of human brucellosis in Hong Kong: a case series in two regional hospitals
S Luk, WK To
Department of Pathology, Princess Margaret Hospital, Laichikok, Hong Kong
 
 
A retrospective analysis of six patients diagnosed with brucellosis in two regional hospitals was carried out. The epidemiological, clinical, and laboratory features were studied. All patients had exposure history. Three patients presented with musculoskeletal symptoms, while three had predominantly genitourinary symptoms. One patient did not have fever at presentation. All patients were diagnosed by positive blood culture of Brucella melitensis, and the diagnosis was not suspected for all except one patient at presentation. Given the inferior sensitivity of blood culture to serology, human brucellosis may be underdiagnosed, especially when the index of suspicion is low.
 
Key words: Anti-bacterial agents; Brucella melitensis; Brucellosis
 
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Probiotics: current trends in the treatment of diarrhoea

ABSTRACT

Hong Kong Med J 2010;16:213-8 | Number 3, June 2010
MEDICAL PRACTICE
Probiotics: current trends in the treatment of diarrhoea
Sujatha S Narayan, Sharmila Jalgaonkar, S Shahani, Vijaya N Kulkarni
K J Somaiya Medical College, Sion, Mumbai, India
 
 
In recent years, research into and public interest in probiotics and probiotic foods have risen. Lactobacilli and bifidobacterium are the most commonly used probiotics while yoghurt and kefir are popular foods containing probiotics. Probiotics have been used to manage diarrhoea. Many things cause diarrhoea, including bacterial, viral and protozoal infections, radiation and antibiotic therapy. Different studies have found that probiotics may also enhance the immune response, reduce serum cholesterol, prevent colonic cancer, prevent dental caries, prevent ulcers due to Helicobacter pylori, maintain urogenital health, and ameliorate hepatic encephalopathy. Further studies are required to establish their role in these conditions.
 
Key words: Bifidobacterium; Clostridium difficile; Diarrhea; Lactobacillus; Probiotics
 
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Laparoscopic management of three rare types of ectopic pregnancy

ABSTRACT

Hong Kong Med J 2010;16:132-6 | Number 2, April 2010
MEDICAL PRACTICE
Laparoscopic management of three rare types of ectopic pregnancy
CM Yan
Department of Obstetrics and Gynaecology, Hong Kong Baptist Hospital, Waterloo Road, Hong Kong
 
 
The laparoscopic management of three rare types of ectopic pregnancy, including rudimentary horn pregnancy, caesarean scar pregnancy, and interstitial pregnancy is described. All were managed with little morbidity. When the appropriate facilities and skills are available, laparoscopic surgery is the surgical treatment of choice for the various types of ectopic pregnancy.
 
Key words: Cesarean section; Laparoscopy; Pregnancy, ectopic; Pregnancy, tubal; Uterine rupture
 
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Transcatheter embolisation of intrahepatic arteriovenous shunts in patients with hepatocellular carcinoma

ABSTRACT

Hong Kong Med J 2010;16:48-55 | Number 1, February 2010
MEDICAL PRACTICE
Transcatheter embolisation of intrahepatic arteriovenous shunts in patients with hepatocellular carcinoma
Winnie SW Chan, WL Poon, Danny HY Cho, Sonny SH Chiu, SH Luk
Department of Radiology, Tuen Mun Hospital, Tuen Mun, New Territories, Hong Kong
 
 
This paper assesses the feasibility of transcatheter embolisation of arteriovenous shunts in patients with hepatocellular carcinoma, and reviews available embolic agents, based on our experience and a literature review. From 2001 to 2007, 11 patients with unresectable hepatocellular carcinoma and significant arteriovenous shunts underwent transcatheter embolisation of liver arteriovenous shunts. The age range was 36 to 80 years. A total of 17 embolisations were performed using different embolic agents including absolute ethanol (n=11), histoacryl (n=1), coils (n=2), and polyvinyl alcohol particles (n=1). We reviewed the degree of shunt occlusion and the clinical outcomes. There were 15 arteriovenous shunts. Nine (60%) were arterioportal venous shunts and six were arteriohepatic venous shunts. Two were classified as 'simple' types, according to our protocol, and 13 were 'complex' types. More than 80% occlusion was achieved in 80% of the shunts. In the simple shunts, coil embolisation achieved complete occlusion. In complex shunts with multiple feeders and draining veins, liquid or particulate agents were required to achieve satisfactory occlusion. Managing arteriovenous shunts with embolisation was feasible. The choice of embolic agent should be based on good understanding of the underlying mechanism of the shunts and their angio-architecture.
 
Key words: Arteriovenous fistula; Carcinoma, hepatocellular; Chemoembolization, therapeutic
 
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Magnetoencephalography and its role in evaluation for epilepsy surgery

ABSTRACT

Hong Kong Med J 2010;16:44-7 | Number 1, February 2010
MEDICAL PRACTICE
Magnetoencephalography and its role in evaluation for epilepsy surgery
TL Poon, FC Cheung, Colin HT Lui
Department of Neurosurgery, Queen Elizabeth Hospital, 30 Gascoigne Road, Kowloon, Hong Kong
 
 
Magnetoencephalography is a newly developed technology used for diagnostic and brain mapping imaging during the presurgical evaluation of patients with medically intractable epilepsy. It provides comprehensive localisation of an epileptogenic focus using simultaneous recordings from the entire brain surface. Magnetoencephalography and electroencephalography are considered complementary and confirmatory to one another. We present a patient with magnetic resonance imaging-negative, non-lesional, neocortical epilepsy. Magnetoencephalography was used for re-evaluation of the epileptogenic zone and this enabled subsequent surgical removal of the epileptic focus. The role of magnetoencephalography in epilepsy surgery is discussed in this report.
 
Key words: Epilepsy/surgery; Magnetoencephalography; Preoperative care
 
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Use of urinary steroid profiling for diagnosing and monitoring adrenocortical tumours

ABSTRACT

Hong Kong Med J 2009;15:463-70 | Number 6, December 2009
MEDICAL PRACTICE
Use of urinary steroid profiling for diagnosing and monitoring adrenocortical tumours
SC Tiu, Angel OK Chan, Norman F Taylor, CY Lee, PY Loung, CH Choi, CC Shek
Department of Medicine, Queen Elizabeth Hospital, 30 Gascoigne Road, Kowloon, Hong Kong
 
 
It has been suggested that urinary steroid profiling may be used to provide information aiding the diagnosis and monitoring of adrenocortical carcinoma. Nonetheless, the abnormal patterns suggestive of adrenal malignancy are not well defined. We retrospectively studied the urinary steroid profiles of five patients with adrenocortical carcinoma at presentation and at follow-up, and compared these results with those from 76 patients with benign adrenocortical adenoma and 172 healthy controls. Three abnormal patterns of urinary steroid excretion were identified in patients with adrenocortical carcinoma at presentation and/or follow-up of residual disease: (1) hypersecretion in multiple steroid axes; (2) excretion of unusual metabolites, notably 5-pregnene-3alpha,16alpha,20alpha-triol, 5-pregnene-3beta,16alpha,20alpha-triol, and neonatal steroid metabolites in the post-neonatal period; (3) increase of tetrahydro-11-deoxycortisol relative to total cortisol metabolites. These preliminary findings offer ways in which urinary steroid profiling performed using gas chromatography-mass spectrometry can be helpful in the diagnosis and monitoring of adrenocortical carcinoma.
 
Key words: Adrenocortical adenoma; Adrenocortical carcinoma; Steroids/urine
 
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BCR-ABL mutational studies for predicting the response of patients with chronic myeloid leukaemia to second-generation tyrosine kinase inhibitors after imatinib failure

ABSTRACT

Hong Kong Med J 2009;15:365-73 | Number 5, October 2009
MEDICAL PRACTICE
BCR-ABL mutational studies for predicting the response of patients with chronic myeloid leukaemia to second-generation tyrosine kinase inhibitors after imatinib failure
TK Kwan, Edmond SK Ma, YY Chan, Thomas SK Wan, Herman SY Liu, Joycelyn PY Sim, YM Yeung, Albert KW Lie, SF Yip
Department of Pathology, Queen Mary Hospital, Pokfulam Road, Hong Kong
 
 
Imatinib is the standard treatment for chronic myeloid leukaemia. BCR-ABL kinase domain mutation is the commonest mechanism implicated in imatinib resistance. In in-vitro studies, kinase domain mutations are variably resistant to second-line agents. We performed BCR-ABL kinase domain mutational studies in 25 patients in five institutions who failed imatinib and were treated with either nilotinib or dasatinib, to see if their mutational status would predict their clinical responses. Kinase domain mutations involving 11 amino acid substitutions were found in 12 (48%) patients. Most patients showed single kinase domain mutations. There was some concordance between reported drug sensitivity patterns and patient responses. Discordant responses could be related to drug dosage variations and unknown BCR-ABL independent mechanisms. The response prediction for patients with multiple kinase domain mutations was challenging and their mutational patterns could change after tyrosine kinase inhibitor therapy. Although BCR-ABL kinase domain mutational analysis has limitations as a means of predicting the clinical response to second-line tyrosine kinase inhibitors, it helps inform therapy decisions in the management of chronic myeloid leukaemia after imatinib failure.
 
Key words: Leukemia, myelogenous, chronic, BCR-ABL positive; Mutation; Protein kinase inhibitors; protein-tyrosine kinases
 
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Refractory thrombotic thrombocytopenic purpura and membranoproliferative glomerulonephritis successfully treated with rituximab but associated with hepatitis B virus infection

ABSTRACT

Hong Kong Med J 2009;15:201-8 | Number 3, June 2009
MEDICAL PRACTICE
Refractory thrombotic thrombocytopenic purpura and membranoproliferative glomerulonephritis successfully treated with rituximab but associated with hepatitis B virus infection
SK Mak, KY Lo, MW Lo, SF Chan, KC Lo, YY Wong, Gensy MW Tong, PN Wong, Edmond SK Ma, Andrew KM Wong
Renal Unit, Department of Medicine and Geriatrics, Kwong Wah Hospital, Kowloon, Hong Kong
 
 
Plasmapheresis remains the main treatment modality for patients with thrombotic thrombocytopenic purpura. We report a patient who had simultaneous onset of membranoproliferative glomerulonephritis and thrombotic thrombocytopenic purpura. She did not improve after 48 plasmapheresis sessions. A 6-week course of weekly intravenous doses of rituximab was then given. This achieved complete remission of her nephrotic syndrome and improvement in her renal function, so plasmapheresis was ceased. She had a low ADAMTS13 antigen level and a positive ADAMTS13 antibody, both of which reverted to normal after treatment with rituximab. This coincided with a rise in her hepatitis C virus RNA and liver transaminases. Liver biopsies did not reveal active fibrosis. Her hepatitis C virus RNA titre dropped afterwards, and she had no relapses of her thrombotic thrombocytopenic purpura and nephrotic syndrome, for more than 2 years after remission. The simultaneous onset and successful outcomes of both the membranoproliferative glomerulonephritis and thrombotic thrombocytopenic purpura illustrate the usefulness of rituximab. We discuss its use and risks, in the context of chronic hepatitis C infection.
 
Key words: Glomerulonephritis, membranous; Hepatitis C; Purpura, thrombocytopenic, idiopathic; Rituximab; Thrombocytopenia
 
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Diagnosis of 5alpha-reductase 2 deficiency: a local experience

ABSTRACT

Hong Kong Med J 2009;15:130-5 | Number 2, April 2009
MEDICAL PRACTICE
Diagnosis of 5alpha-reductase 2 deficiency: a local experience
Angel OK Chan, Betty WM But, Gene TC Lau, Almen LN Lam, KL Ng, YY Lam, CY Lee, CC Shek
Department of Pathology, Queen Elizabeth Hospital, Gascoigne Road, Hong Kong
 
 
5Alpha-reductase 2 deficiency is an autosomal recessive disorder characterised by lack of masculinisation in XY individuals due to failure to convert testosterone to dihydrotestosterone, the bioactive androgen. Traditionally, the testosterone-to-dihydrotestosterone ratio is used to diagnose this condition but interpreting these results is not always straightforward, thus they may be inconclusive. On the contrary, urinary steroid profiling unambiguously demonstrates a significantly reduced excretion of 5alpha-reduced steroid metabolites compared to their 5beta counterparts. This analytical technique can also simultaneously confirm or rule out other causes of ambiguous genitalia due to steroidogenic defects. Making a DNA-based diagnosis by studying the SRD5A2 gene has become increasingly popular. Here, we report six Chinese patients from different families who were all diagnosed with 5alpha-reductase 2 deficiency based on urinary steroid profile findings and mutational analysis of the SRD5A2 gene. R227Q was the most commonly identified mutation in these patients. Management of sexual development disorders is also discussed.
 
Key words: Dihydrotestosterone; Genitalia; Mutation; Testosterone 5-alphareductase
 
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