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The Turkish Journal of Gastroenterology |
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91-93 |
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To the Editor
A rare cause of lymphadenopathy near the
terminal ileum: immunoproliferative small
intestinal disease |
| Chun-Chao HUANG, Chin-Yin SHEU |
| Department of Radiology, Mackay Memorial Hospital, Taipei,
Thaiwan, Republic of China |
| Introduction |
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To the Editor,
Immunoproliferative small intestinal disease (IPSID)
is a subtype of mucosa-associated lymphoid
tissue (MALT) lymphoma. Campylobacter jejuni is
suspected in the etiology. The most frequently affected sites are the duodenum and upper jejunum.
To date, long-term antibiotic therapy has been the
first-line treatment for early and late stage 0 in a
staging system proposed by Salem and Estephan,
and then chemotherapy is the next choice. In contrast,
surgery is reserved for staging and uncommon
abdominal disasters (1,2).
A 53-year-old woman had stage IA endometrial
adenocarcinoma, FIGO grade 1, and underwent a
staging operation. One year after the initial diagnosis
of endometrial cancer, pelvic sonography showed
ascites. At that time, this patient complained
of mild intermittent abdominal distention and lower
abdominal discomfort. Apart from these symptoms,
she denied having weight loss, chronic diarrhea,
nausea, or fever, etc. Computed tomography
(CT) showed a 3.7-centimeter conglomerate mass
as well as multiple nodules nearby and focal fat
stranding in the mesentery of the right lower quadrant,
close to the terminal ileum (Figure 1). Aside
from these abnormalities, there were no other significant
findings in any other region. Another CT
six weeks later displayed that the above-mentioned
lesions had grown slightly. There was no important
abnormality in the basic laboratory data.
Metastasis of endometrial cancer was originally
considered as the primary cause of these lesions,
but a few differential diagnoses such as lymphoma
or inflammatory diseases were also contemplated.
In order to reach a definite diagnosis, exploratory
laparotomy was performed, and multiple nodules
in the mesocolon of the ascending colon were found.
The frozen section report showed lymphoid
tissue proliferation but lymphoma could not be ruled
out. Since the possibility of malignancy could
still not be excluded, right hemicolectomy was carried
out. The pathology report confirmed the final
diagnosis as IPSID, late stage 0.
The history of malignancy initially lured us into
attributing these lesions to metastasis. However,
for lesions near the terminal ileum, there are various
differential diagnoses, ranging from malignant
to benign entities (3). Primary small intestinal
lymphoma was the second impression in this
patient because of the patient’s age and the affected
location of the lymphadenopathy. However, focal
clustered enlarged lymph nodes are not typical
for metastasis or primary small intestinal lymphoma
(1,4). Therefore, retrieving more problematic
tissue by surgical biopsy might have been a better
choice for this patient because this would have given
the patient the opportunity to receive antibiotic
treatment or chemotherapy instead of right hemicolectomy. |
Top
Introduction
References
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| References |
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1. Salem P, el-Hashimi L, Anaissie E, et al. Primary small intestinal
lymphoma in adults: a comparative study of IPSID
versus non-IPSID in the Middle East. Cancer 1987; 59:
1670-6.
2. Salem PA, Estephan FF. Immunoproliferative small intestinal
disease: current concepts. Cancer J 2005; 11: 374-82.
3. Hoeffel C, Crema MD, Belkacem A, et al. Multi-detector
row CT: spectrum of diseases involving the ileocecal area.
Radiographics 2006; 26: 1373-90.
4. Mendelson RM, Fermoyle S. Primary gastrointestinal
lymphomas: a radiological-pathological review. Part 2:
Small intestine. Australas Radiol 2006; 50: 102-13. |
Top
Introduction
References
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