Online
Clinical Case Study (April
2006)
Clinical
Cardiology Series
臨床心臟科個案研究
The
content of the Office Cardiology Series is provided by:
Dr. SO Yui Chi
M.B.,B.S.(H.K.), M.R.C.P.(U.K.), M.R.C.P.(Ireland), F.H.K.C.P.,
F.H.K.A.M. (Med), Specialist in Cardiology
Dr. LI Siu Lung, Steven
M.B.,B.S.(H.K.), M.R.C.P.(U.K.), F.H.K.A.M., F.H.K.C.P., F.R.C.P.(Glasg.),
F.R.C.P.
(Edin.), Specialist in Cardiology
Dr. WONG Shou Pang, Alexander
F. R.C.P., F.H.K.A.M.(Med.), F.H.K.C.P., Specialist in Cardiology
臨床心臟科個案研究之內容誠蒙蘇睿智醫生、李少隆醫生及王壽鵬醫生提供。

Mr. Chan was following
up in a psychiatric clinic for his depression. He was on regular drug treatment.
He visited our ER room for repeated loss of consciousness. He was transferred
to the ward with the cardiac monitor tracing below:
Answers
| 1. |
What
is the underlying cause of Mr. Chan's loss of consciousness?
a) Vasovagal attack
b) Atrial fibrillation
c) Asystole
d) Polymorphic VT
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d.
Mr. Chan has a polymorphic VT attack. It was started with an increase
of QT interval (0.46 sec) and there was a ventricular ectopic (VE) which
caused a pause. The spontaneous sinus rhythm that followed the VE had
an R on T phenomenon by the subsequent VE and the whole polymorphic VT
was started.
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| 2. |
What
is your management plan?
a) Check the electrolytes
b) Check the drugs
c) IV lignocaine
d) Pacing
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a,b and
d. Because of the long QT interval, we should try to correct any disturbance
in the electrolytes including those of potassium, magnesium and calcium.
A temporary pacemaker to accelerate the spontaneous sinus rhythm would
be very useful as it corrects the QT interval and suppresses the ventricular
ectopics. The whole ventricular event can then be stopped. This patient
was on tricyclic anti-depressants (TCA) and the drug had caused the QT
interval prolongation. His electrolytes were normal. His VT storm was
finally stopped by pacing and his TCA was stopped. QT intervals should
be monitored regularly in patients who were put on TCA.
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Dermatology
Series 皮膚科病例研究
A 35 year old Australian
male presented with an enlarging pigmented nodule over his back for three months.
The nodule developed from a pre-existing congenital mole and was non-itchy and
non-painful. Physical examination showed a one centimeter size dark black firm
nodule at his back with pigmentation spreading beyond the margin of the nodule.
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The
content of the Dermatology Series is provided by:
Dr. KU Lap Shing, Simon; Dr. CHAN Loi Yuen & Dr. TANG Yuk
Ming, William
Specialist in Dermatology & Venereology
皮膚科病例研究之內容誠蒙顧立誠醫生、陳來源醫生及鄧旭明醫生提供。 |
Answers
| 1. |
What
are the clinical diagnosis and differential diagnoses?
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The most likely diagnosis
is a malignant melanoma arising from a pre-existing mole. The differential
diagnoses are pigmented basal cell carcinoma, pyogenic granuloma, haemagioma,
and cutaneous secondary metastasis.
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| 2. |
What
are the predisposing factors?
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The predisposing factors for
malignant melanoma include the presence of precursor lesions like dysplastic
nevi, congenital nevomelanocytic nevi; family history of melanoma in parents,
children and siblings; light skin type with inability to tan easily; and
excessive sun exposure, especially during childhood. The estimated life-time
melanoma risk for congenital nevomelanocytic nevi smaller than and bigger
than 10 cm in diameter are 0-4.9% and 4.5-10% respectively.
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| 3. |
How
would you confirm the diagnosis?
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Total excisional biopsy should
be performed. However, in case of a large lesion, an incisional biopsy
can be performed to establish the diagnosis but this may result in sampling
error and false negative finding.
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| 4. |
What
are the prognostic factors?
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The prognosis depends on the
clinical staging. Tumor thickness as denoted by the Clark level and the
Breslow thickness are important prognostic factors.
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| 5. |
What
is the management and what are the important investigations for evaluating
the disease?
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Wide margin re-excision remains
the mainstay of treatment. Extensive work-up including sentinel lymph
node biopsy, positron emission tomography scan should be performed for
staging of the disease. Depending on the clinical stage, further interventions
like single or combination chemotherapy, systemic interferon, biologics,
chemo-immunotherapy, gene therapy or radiotherapy for palliative treatment
of metastasis may be tried.
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