Fever of unknown origin (FUO) was defined in 1961
as:
-
A temperature greater than 38.3°C (101°F) on several occasions,
-
More than 3 weeks' duration of illness, and
-
Failure to reach a diagnosis despite 1 week of inpatient investigation.
Now, most of diseases that may cause continuous
fever and dilemma in arriving at diagnosis decreased after the advent
of various imaging and investigative technologies.
The most
common causes of FUO like tuberculosis, collagen
diseases, AIDS and malignancies can be diagnosed by newer serological
tests, ultrasonogram, CT, MRI and PET/CT etc..
In spite of all these, there may be occasions,
where it may not be possible to differentiate mesenteric
lymphadenopathay of lymphoma and tuberculous aetiology without any
other associated features.
Intra-Abdominal Lymph Nodes |
In multi-detection computerized tomography (MDCT),
it has been seen that lymphadenopathy of tuberculous origin mostly
affect the LN (Lymph node) adjacent to the intestinal mesenteric
boarder, where as in lymphoma more distant LN like para-aortic are
involved.
Tuberculosis predominantly involved lesser
omental, mesenteric, and upper para-aortic lymph nodes whereas lower
para-aortic lymph nodes were involved more often in Hodgkin’s and
non-Hodgkin’s lymphoma.
Peripheral enhancement is most commonly seen in tuberculosis, whereas homogeneous enhancement is seen in lymphoma.
The contrast enhancement of tuberculous lymph
nodes on contrast-enhanced CT (CECT) have been described as (four
patterns) - peripheral rim enhancement, inhomogeneous enhancement, homogeneous enhancement and homogeneous non-enhancement, in that order
of frequency.
'Sand-witch'
sign, encasing of superior mesenteric vessels and fat (Filling) by
the lymph node mass as “Bun” is most commonly seen in lymphoma.
In a study, the mean diameters
were 2.95 cm in tuberculous lymphadenopathy, whereas it was 4.10 cm
in lymphoma.
Associated
findings like thickening of intestine, ascites and peritoneal
thickening are more commonly seen in tuberculosis.
In spite of
all, a CT/USG guided FNAC or laparoscopic tissue
diagnosis is required for the final diagnosis and treatment planning.