![]() Issue No. 6, Jul 2009 |
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Issue No. 6 - Jul 2009 | ||
Pages | ||
8-16 | PET and PET/CT in the Clinical Management of Colorectal Cancer | |
T. El-Maghraby Nuclear Medicine Section, Saad Specialist Hospital, Al-Khobar, Saudi Arabia |
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Abstract | ||
PET/CT is a new
imaging technology that has already
found a number of clinical applications
in oncologic imaging. Widespread
introduction into clinical practice
started approximately 5 years ago. It
can already be stated that the synthesis
of structural and metabolic information
improves the accuracy of primary staging
and the detection of recurrent disease
and has the realistic potential to
change patient management in up to 30%
of cases. PET/CT imaging of Colorectal
Malignancies has shown that this new
modality has higher specificity and
sensitivity than PET alone and in
certain settings even when compared to
PET and CT viewed side by side. Ongoing
and future studies will refine its exact
place in the diagnostic work-up of
colorectal cancer patients and address
how often PET/CT can eliminate the need
for other imaging studies that are
currently performed for the staging or
detection of recurrence in these
patients. PET/ CT fusion images can
directly guide biopsies or surgical
interventions. This manuscript
highlights on potential clinical
applications for PET/CT in colorectal
tumors. |
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full article | ||
2 | 17-27 | Conformal Radiation Therapy in Prostate Cancer - A Review |
A. Varghese,
A. Juzer Department of Radiation Oncology, Kuwait Cancer Control Centre |
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Abstract | ||
Purpose Radiotherapy
has progressed considerably over a
century. It is mainly because of
understanding of physical and biological
principles. How to improve therapeutic
ratio is major concern. Excellent dose
conformality and homogeneity is possible
due to recent advances in treatment
techniques. But there are many areas of
challenges in achieving increased tumor
control and normal tissue effects. The
aim of this review is to provide a brief
update of the rapidly changing field of
external radiotherapy and how it affects
the clinical practice of treatment of
prostate cancer. |
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full article | ||
3 | 28-34 | Cervical Cancer Screening among Sudanese Women |
F. M. Hassan,
M. KhirElseed |
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Abstract | ||
Worldwide, cervical
cancer is one of the three most common
female cancers and accounts for over
370,000 new cases each year ( nearly 10%
of all cancers). In Sudan, invasive
cervical cancers is a leading cause of
cancer death among women. |
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full article | ||
4 | 35-40 | Assessment of Three-Dimensional Set-up Errors in Head and Neck Cancer Patients Treated by Intensity Modulated Radiotherapy using Electronic Portal Imaging Device |
Y. Bayoumi,
A. Al-Amro, R. A. Moniem, I. Sohaibani,
O. Al-hanafy, A. S. Alawadi, M. Asiri Radiation Oncology Department, Prince Sultan Haematology Oncology Center, King Fahad Medical City, Riyadh, Saudi Arabia |
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Abstract | ||
Set-up errors are an
inherent part of radiation treatment
process. Coverage of target volume is a
direct function of set-up margins, which
should be optimized to prevent
inadvertent irradiation of adjacent
normal tissues. The aim of this study is
to evaluate set-up errors and propose
optimum margins for target volume
coverage in head and neck radiotherapy.
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full article | ||
5 | 41-44 | Comparison of Bone Marrow Aspiration and Bone Marrow Biopsy in Neoplastic Diseases |
G. A. Hamid1 and N.
Hanbala2 |
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Abstract | ||
Naturally trephine
biopsies have definitive advantages over
aspirates in case of dry tap bone marrow
aspirates as a result of fibrosis or
densely packed bone marrow by tumour
cells and may be informative independent
of cytology especially in bone marrow
involvement by lymphomas and carcinomas.
In this prospective descriptive study we
aimed to compare between the bone marrow
trephine biopsy (BMTB) and bone marrow
aspirates (BMAs) regarding the detection
rate of solid tumours, lymphoma and
myeloma involvement of the bone marrow.
The study was carried out in the
department of pathology and Haematology-Oncology
of Al-Gamhouria Teaching Hospital/Aden
during the period between Jan 2005 to
Dec 2005 . A total of 32 patients with
suspected or confirmed malignancy
undergone both BMTB and BMA from the
posterior superior iliac crest and both
results were compared. We divided them
into three groups: those with solid
tumours (21) patients, lymphoma (7)
patients and with MM (4) patients. Our
results showed that BMA had a 47.6%
sensitivity, 100.0% specificity, with
positive predictive value (100%), and
negative predictive value (50.0%). In
solid tumours alone it had a sensitivity
of (40.0%), 100% specificity, with
positive predictive value (100%), and
negative predictive value (64.7%). This
gives the BMA a lower sensitivity in
detecting solid tumour metastasis and
lymphoma involvement in comparison to
BMTB. In conclusion, any patient with
suspected or confirmed cancer should
undergo BMTB because of its high
sensitivity compared to BMA. |
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full article | ||
6 | 45-47 | Cervical Neonatal Neuroblastoma with Recurrent SVT |
N. F. Al-Shammari,
E. Redha, M. H. Al Hajeri |
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Abstract | ||
Neuroblastoma is the
most common extracranial solid tumor of
childhood and the third most common
paediatric malignancy after leukemia and
central nervous system(CNS) tumors. It
constitutes 10% of all paediatric
malignancies and 75% of them present in
children below 4 years of age. Seventy
five percent of neuroblastoma arise in
the abdomen and pelvis, 20% in the
thorax and 5% in the neck. The median
age at diagnosis is 22 months. Up to 95%
of cases are diagnosed by the age of ten
years. Neuroblastomas have been
diagnosed in utero as early as 19 weeks
of gestational age. They can arise
anywhere along the sympathetic chain.
They occur most commonly in the adrenal
medulla (35%). Neuroblastomas also occur
as primary tumors in the extra-adrenal
retroperitoneum in 30% of cases, in the
posterior mediastinum in 20% of cases ,
in the neck up to 5% of cases and in the
pelvis in 5% of cases. Approximately 50%
of patients will have metastasis at
presentation. |
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full article | ||
7 | 48-50 | Multicentric Castleman Disease: Report of Rare Disease in Kuwait |
B. A.
Mohammad¹, N. Al-Brahim², S.
Kunjhibava¹, M. Ahmad² ¹Department of Medicine, ²Department of Pathology, Al-Farwaniya Hospital, Kuwait |
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Abstract | ||
We report a rare case
of multicentric Castleman disease
diagnosed in Kuwait. A 56-year-old man
presented with fever of unknown origin
and generalized lymphadenopathy.
Laboratory investigations revealed mild
anemia and polyclonal gammopathy. Bone
marrow biopsy demonstrated 15% increase
in plasma cells. Viral screenings
including HIV were negative. Lymph node
biopsy showed follicular hyperplasia
with inter-follicular plasma cells
infiltrate with a typical morphology of
plasma cell variant of Castleman
disease. The patient was treated with
methyl-prednisone pulse therapy and
showed good response. |
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full article | ||
8 | 51-55 | Significance of Intracytoplasmic Crystalline Inclusions in Plasma Cells – A Review with Case Discussion |
R. Arora, A.
A. El-Hameed, T. Al Ajrawi
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Abstract | ||
Dense
lymphoplasmacytic infiltrate in tissues
pose diagnostic challenge to
pathologists. Presence of
intracytoplasmic crystalline inclusions
in plasma cells has been strongly linked
with B- cell lymphoproliferative
disorders, although isolated reactive
cases are also reported. We reviewed the
literature and present clinical,
morphological and immunohistochemical
findings in a polyp of the cervix. The
polyp showed extensive plasma cell
infiltrate with needle shaped and
elongated intracytoplasmic inclusions in
many of them. These cells were positive
for CD 79α, CD 138 , kappa and lambda
light chain ( equal proportions) and IgG.
They were negative for cytokeratin,
desmin, CD 20, CD 68, and IgA.
Immunoprofile, laboratory data and
clinical follow up were consistent with
reactive nature of the lesion. This case
highlights the fact that the presence of
intracytoplasmic crystalline inclusions
should not be considered pathognomonic
of B-cell lymphoproliferative disorder.
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full article | ||
9 | 56-59 | Primary Xanthoma of The Acromion: A Case Report and Review of the Literature |
H. S. Alsaif1,
K. M.Moghazy1, M. M. Asiri1,
M. A. El-Shawarby2
Departments of 1 Radiology, and 2 Pathology college of Medicine, King Faisal University, Dammam, King Fahad Hospital of the University, Al-khobar, Saudi Arabia |
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Abstract | ||
Primary “xanthoma” of
bone is a rare lesion of unsettled
histogenesis that may pose a diagnostic
challenge owing to its wide range of
differential diagnosis. Herein, we
present a case of primary xanthoma of
the right acromion in a middle aged
woman who had no aberrant lipid
metabolism or evidence of other
pre-existing bone lesions. To our
knowledge, this is the second reported
case of a primary xanthoma involving the
acromion in an adult. |
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full article | ||