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eCommons@AKU
Department of Radiology Medical College, Pakistan
January 2017
Autoimmune Disease Presenting As Acute
Abdomen
Wasim A Memon
Aga Khan University, wasim.memon@aku.edu
Saad Siddiqui
Aga Khan University, saad.siddiqui@aku.edu
Ameer Hamza
Aga Khan University, hamza.ameer@aku.edu
Follow this and additional works at: https://ecommons.aku.edu/pakistan_fhs_mc_radiol
Part of the Radiology Commons
Recommended Citation
A Memon, W., Siddiqui, S., Hamza, A. (2017). Autoimmune Disease Presenting As Acute Abdomen. Journal of Ayub Medical College,
29(1), 139-141.
Available at: https://ecommons.aku.edu/pakistan_fhs_mc_radiol/153
brought to you by CORE
View metadata, citation and similar papers at core.ac.uk
provided by eCommons@AKU
J Ayub Med Coll Abbottabad 2017;29(1)
http://www.jamc.ayubmed.edu.pk 139
CASE SERIES
AUTOIMMUNE DISEASE PRESENTING AS ACUTE ABDOMEN
Wasim A. Memon, Saad Siddiqui, Ameer Hamza
Department of Radiology, Aga Khan University Karachi-Pakistan
Mesenteric vasculitis and resultant bowel ischemia is rare but serious complication of autoimmune
disorders. Early detection and treatment is the key to avoid potentially fatal outcomes of bowel
perforation and peritonitis. In this series, we present patients presenting with acute abdominal pain
and having CT imaging features of bowel ischemia who responded well to immunosuppressive
therapy. The aim of this work is to familiarize health professionals with possibility and imaging
features of mesenteric vasculitis.
Keywords: Acute abdomen; Autoimmune; Laparatomy; Vasculitis; Bowel ischemia; Mesenteric
vasculitis
J Ayub Med Coll Abbottabad 2017;29(1):139–41
INTRODUCTION
Vasculitis syndromes usually result in
noninfectious inflammation of blood vessels.
Various syndromes have predilection for different
sized blood vessels and although rare in
incidence, many of them can present with a wide
spectrum of symptomatology. Vasculitis
syndromes can involve any part of the body with
classic and rare presentations. Autoimmune
disorders particularly systemic lupus erythematosus
(SLE) can lead to vasculitis of gastrointestinal tract
with presentations like abdominal pain, nausea,
vomiting and loose stools. The associated findings
could include severe serositis, enteritis, and
pancreatitis and bowel ischemia leading to
perforation.1,2
The unusual presentations of ischemic
bowel changes as a result of mesenteric vasculitis
pose a diagnostic challenge. In patients with already
known underlying autoimmune disease, a
presentation of acute abdomen with or without signs
of peritonitis should always raise concern of bowel
ischemia secondary to mesenteric vasculitis. The
role of computed tomography (CT scan) has
recently been highlighted in literature as an
efficient tool in diagnosis of mesenteric vasculitis
and resulting inflammatory & ischemic changes.3
In this work we would like to describe a series of
patients with acute abdomen secondary to
mesenteric vasculitis and resultant changes in
bowel.
CASE 1
A 32-year-old lady presented to emergency room
(ER) with complains of severe abdominal pain
and loose stools for past 6 days. Her past medical
history was positive for Systemic Lupus
Erythematosus and seronegative polyarthritis. She
was not taking any active medications at time of
presentation. On examination, she was afebrile
with a blood pressure of 114/70 mm Hg, Pulse
rate of 140 beats per minute and a respiratory rate
of 24 breaths per minute.
Systemic examination revealed distended
abdomen with rigidity, rebound tenderness in
epigastrium and absent bowel sounds. A contrast
enhanced CT scan of the abdomen and pelvis was
performed which revealed diffusely thick walled,
oedematous and mildly dilated small bowel along
with surrounding fat haziness and peripheral
enhancement. The findings were giving
characteristic target appearance without evidence of
intramural air. The top differential of this
appearance was bowel ischemia however there was
no evidence of thrombus in superior mesenteric
artery or vein (Figure-1). The patient was started on
pulse dose of Methyl prednisolone and responded
well to it. The complaints of abdominal pain and
rigidity resolved and patient was discharged home
on Immunosuppressive treatment.
Figure-1: Thickened and enhancing small bowel loops with target appearance. Associated serositis has
resulted in ascites
J Ayub Med Coll Abbottabad 2017;29(1)
http://www.jamc.ayubmed.edu.pk
140
CASE 2
A 16-year-old lady presented to emergency room
with complaints of severe abdominal pain and
vomiting for past 15 days. Her past medical history
was positive for Systemic Lupus Erythematosus and
before presenting to our institute she was
conservatively managed in a peripheral hospital
with provisional diagnosis of intestinal obstruction.
She was not on any active treatment for SLE at time
of presentation. On examination, she was afebrile
with a blood pressure of 128/80 mm Hg, Pulse rate of
89 beats per minute and a respiratory rate of 20
breaths per minute. Systemic examination revealed
diffusely tender abdomen with hyper resonant note
on percussion and sluggish gut sounds. An initial
impression of sub-acute intestinal obstruction was
made and management started on its lines.
A contrast enhanced CT scan of Abdomen
was ordered which revealed; abnormal differential
enhancement of almost the entire small bowel loops
without any significant dilatation. Normal
mesenteric vasculature was seen without evidence
of thrombosis; the findings were consistent with
bowel ischemia (Figure-2). The patient was
administered methyl prednisolone as pulse therapy
and responded well to it. The complaints subsided,
she was started enteral feeding which she tolerated
well and subsequently was discharged from hospital.
Figure-2: Oedematous small bowel loops with differential enhancement. Associated serositis has resulted in ascites
CASE 3
A 55 years old gentleman presented to emergency
room with history of abdominal pain, purpura and
pruritus for 15 days. He had no previously known
comorbidities. On examination, he was afebrile with
a blood pressure of 130/80 mm Hg, heart rate of 110
beats per minute and respiratory rate of 18 breaths
per minute. Systemic examination revealed a soft,
diffusely tender abdomen. After initial resuscitation
contrast, enhanced CT scan of abdomen was
performed to evaluate the abdominal pain. The
findings of this scan revealed abnormal wall
thickening with dilatation of the proximal jejunum,
distal ileum and terminal ileum with associated
involvement of caecum.
The caecum was giving a targeted
appearance. Surrounding fat stranding with
significantly increased vascularity of the arterial
arcades (vasa recta) was also noted giving
appearance of comb sign. Patient was
administered methyl prednisolone as pulse
therapy along with azathioprine and responded
well to it. The complaint subsided and was
subsequently discharged from hospital
.
Figure-3: Abnormal wall thickening of distal small bowel loops including terminal ileum. Note the target
appearance of caecum
J Ayub Med Coll Abbottabad 2017;29(1)
http://www.jamc.ayubmed.edu.pk 141
DISCUSSION
Mesenteric vasculitis is one of the most serious
complications of autoimmune disease particularly
systemic lupus erythematosus. It results in
associated changes of bowel ischemia and mucosal
inflammation leading to enteritis. In severe cases
this may result in bowel perforation and
subsequent peritonitis. The incidence of mesenteric
vasculitis in patients with systemic lupus
erythematosus is reported to be in range of 0.2–53%.
A variety of symptoms have been observed in
patients presenting with underlying autoimmune
process however acute abdominal pain remains to be
the most common presenting feature with reported
frequencies of 33–62%. The cause of acute
abdominal pain can be secondary to involvement of
central nervous system, serositis, enteritis,
pancreatitis, uraemia and primary peritonitis
however mesenteric vasculitis leading to bowel
ischemia remains to be the most serious.1,2,4
Computed Tomography (CT scan) remains
to be the most valuable modality in early diagnosis
of bowel ischemia. The strength of CT scan lies in
its ability to demonstrate bowel wall and mesenteric
vasculature simultaneously. Typically, CT findings
in mesenteric ischemia include abnormal dilatation
of loops with or without wall thickness (this can be
focal or diffuse). Abnormal enhancement which are
classically describe by double halo or target signs.
Mesenteric oedema with prominent vasculature.
Although these signs are sensitive in detection of
bowel ischemia, the downside is their lack of
specificity as they can be seen in a variety of other
disease processes as well. Although intramural air is
a classic finding in bowel ischemia due to
thrombotic episode, it is rare in mesenteric
vasculitis. The same was observed in our patients as
well. Recent literature has also emphasized on the
importance of initial mesenteric vascular
prominence (Comb sign) as an early sign of
mesenteric vasculitis. Similar picture was observed
in one of our patients as well.3,5
Other finding seen on imaging in autoimmune
processes as described in literature include
lymphadenopathy, hepatosplenomegaly,
inflammatory changes of the pancreas, ascites and
renal parenchymal changes. Ascites and pancreatitis
was observed as associated findings in our patients
as well.3
According to findings of established
literature patients usually respond well to high dose
prednisolone therapy with resolution of symptoms.
The same was observed in this series as well. A
surgical intervention is rarely required. Most of the
cases later need to be started on immunosuppressant
therapy by use of agents like Azathioprine and
Cyclophosphamide as relapse is common.2
The
limitation of our series include lack of follow up
scans to assess the extent of resolution of disease
process on imaging.
CONCLUSION
Early diagnosis and management by high dose
steroids is the key to prevent complications in cases
of mesenteric vasculitis. The diagnosis should be
considered in any patient with history of
autoimmune disorder presenting with acute abdomen
or having Imaging features of bowel Ischemia.
REFERENCES
1. Sran S, Sran M, Patel N, Anand P. Lupus enteritis as an
initial presentation of systemic lupus erythematosus. Case
Rep Gastrointest Med 2014;2014:962735.
2. Tian XP, Zhang X. Gastrointestinal involvement in
systemic lupus erythematosus: insight into pathogenesis,
diagnosis and treatment. World J Gastroenterol
2010;16(24):2971–7.
3. Byun JY, Ha HK, Yu SY, Min JK, Park SH, Kim HY, et al.
CT features of systemic lupus erythematosus in patients with
acute abdominal pain: emphasis on ischemic bowel disease.
Radiolog 1999;211(1):203–9.
4. Lee CK, Ahn MS, Lee EY, Shin JH, Cho YS, Ha HK,
et al. Acute abdominal pain in systemic lupus
erythematosus: focus on lupus enteritis (gastrointestinal
vasculitis). Ann Rheum Dis 2002;61(6):547–50.
5. Wiesner W, Khurana B, Ji H, Ros PR. CT of acute
bowel ischemia. Radiology 2003;226(3):635–50.
Received: 14 August, 2015 Revised: 17 May,2016 Accepted: 26 December, 2016
Address for Correspondence:
Dr. Saad Siddiqui, Department of Radiology, The Aga Khan University, Karachi- Pakistan
Cell: +92 321 906 3099
Email: saadsiddiqui.5@gmail.com

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Autoimmune Disease Presenting As Acute Abdomen

  • 1. eCommons@AKU Department of Radiology Medical College, Pakistan January 2017 Autoimmune Disease Presenting As Acute Abdomen Wasim A Memon Aga Khan University, wasim.memon@aku.edu Saad Siddiqui Aga Khan University, saad.siddiqui@aku.edu Ameer Hamza Aga Khan University, hamza.ameer@aku.edu Follow this and additional works at: https://ecommons.aku.edu/pakistan_fhs_mc_radiol Part of the Radiology Commons Recommended Citation A Memon, W., Siddiqui, S., Hamza, A. (2017). Autoimmune Disease Presenting As Acute Abdomen. Journal of Ayub Medical College, 29(1), 139-141. Available at: https://ecommons.aku.edu/pakistan_fhs_mc_radiol/153 brought to you by CORE View metadata, citation and similar papers at core.ac.uk provided by eCommons@AKU
  • 2. J Ayub Med Coll Abbottabad 2017;29(1) http://www.jamc.ayubmed.edu.pk 139 CASE SERIES AUTOIMMUNE DISEASE PRESENTING AS ACUTE ABDOMEN Wasim A. Memon, Saad Siddiqui, Ameer Hamza Department of Radiology, Aga Khan University Karachi-Pakistan Mesenteric vasculitis and resultant bowel ischemia is rare but serious complication of autoimmune disorders. Early detection and treatment is the key to avoid potentially fatal outcomes of bowel perforation and peritonitis. In this series, we present patients presenting with acute abdominal pain and having CT imaging features of bowel ischemia who responded well to immunosuppressive therapy. The aim of this work is to familiarize health professionals with possibility and imaging features of mesenteric vasculitis. Keywords: Acute abdomen; Autoimmune; Laparatomy; Vasculitis; Bowel ischemia; Mesenteric vasculitis J Ayub Med Coll Abbottabad 2017;29(1):139–41 INTRODUCTION Vasculitis syndromes usually result in noninfectious inflammation of blood vessels. Various syndromes have predilection for different sized blood vessels and although rare in incidence, many of them can present with a wide spectrum of symptomatology. Vasculitis syndromes can involve any part of the body with classic and rare presentations. Autoimmune disorders particularly systemic lupus erythematosus (SLE) can lead to vasculitis of gastrointestinal tract with presentations like abdominal pain, nausea, vomiting and loose stools. The associated findings could include severe serositis, enteritis, and pancreatitis and bowel ischemia leading to perforation.1,2 The unusual presentations of ischemic bowel changes as a result of mesenteric vasculitis pose a diagnostic challenge. In patients with already known underlying autoimmune disease, a presentation of acute abdomen with or without signs of peritonitis should always raise concern of bowel ischemia secondary to mesenteric vasculitis. The role of computed tomography (CT scan) has recently been highlighted in literature as an efficient tool in diagnosis of mesenteric vasculitis and resulting inflammatory & ischemic changes.3 In this work we would like to describe a series of patients with acute abdomen secondary to mesenteric vasculitis and resultant changes in bowel. CASE 1 A 32-year-old lady presented to emergency room (ER) with complains of severe abdominal pain and loose stools for past 6 days. Her past medical history was positive for Systemic Lupus Erythematosus and seronegative polyarthritis. She was not taking any active medications at time of presentation. On examination, she was afebrile with a blood pressure of 114/70 mm Hg, Pulse rate of 140 beats per minute and a respiratory rate of 24 breaths per minute. Systemic examination revealed distended abdomen with rigidity, rebound tenderness in epigastrium and absent bowel sounds. A contrast enhanced CT scan of the abdomen and pelvis was performed which revealed diffusely thick walled, oedematous and mildly dilated small bowel along with surrounding fat haziness and peripheral enhancement. The findings were giving characteristic target appearance without evidence of intramural air. The top differential of this appearance was bowel ischemia however there was no evidence of thrombus in superior mesenteric artery or vein (Figure-1). The patient was started on pulse dose of Methyl prednisolone and responded well to it. The complaints of abdominal pain and rigidity resolved and patient was discharged home on Immunosuppressive treatment. Figure-1: Thickened and enhancing small bowel loops with target appearance. Associated serositis has resulted in ascites
  • 3. J Ayub Med Coll Abbottabad 2017;29(1) http://www.jamc.ayubmed.edu.pk 140 CASE 2 A 16-year-old lady presented to emergency room with complaints of severe abdominal pain and vomiting for past 15 days. Her past medical history was positive for Systemic Lupus Erythematosus and before presenting to our institute she was conservatively managed in a peripheral hospital with provisional diagnosis of intestinal obstruction. She was not on any active treatment for SLE at time of presentation. On examination, she was afebrile with a blood pressure of 128/80 mm Hg, Pulse rate of 89 beats per minute and a respiratory rate of 20 breaths per minute. Systemic examination revealed diffusely tender abdomen with hyper resonant note on percussion and sluggish gut sounds. An initial impression of sub-acute intestinal obstruction was made and management started on its lines. A contrast enhanced CT scan of Abdomen was ordered which revealed; abnormal differential enhancement of almost the entire small bowel loops without any significant dilatation. Normal mesenteric vasculature was seen without evidence of thrombosis; the findings were consistent with bowel ischemia (Figure-2). The patient was administered methyl prednisolone as pulse therapy and responded well to it. The complaints subsided, she was started enteral feeding which she tolerated well and subsequently was discharged from hospital. Figure-2: Oedematous small bowel loops with differential enhancement. Associated serositis has resulted in ascites CASE 3 A 55 years old gentleman presented to emergency room with history of abdominal pain, purpura and pruritus for 15 days. He had no previously known comorbidities. On examination, he was afebrile with a blood pressure of 130/80 mm Hg, heart rate of 110 beats per minute and respiratory rate of 18 breaths per minute. Systemic examination revealed a soft, diffusely tender abdomen. After initial resuscitation contrast, enhanced CT scan of abdomen was performed to evaluate the abdominal pain. The findings of this scan revealed abnormal wall thickening with dilatation of the proximal jejunum, distal ileum and terminal ileum with associated involvement of caecum. The caecum was giving a targeted appearance. Surrounding fat stranding with significantly increased vascularity of the arterial arcades (vasa recta) was also noted giving appearance of comb sign. Patient was administered methyl prednisolone as pulse therapy along with azathioprine and responded well to it. The complaint subsided and was subsequently discharged from hospital . Figure-3: Abnormal wall thickening of distal small bowel loops including terminal ileum. Note the target appearance of caecum
  • 4. J Ayub Med Coll Abbottabad 2017;29(1) http://www.jamc.ayubmed.edu.pk 141 DISCUSSION Mesenteric vasculitis is one of the most serious complications of autoimmune disease particularly systemic lupus erythematosus. It results in associated changes of bowel ischemia and mucosal inflammation leading to enteritis. In severe cases this may result in bowel perforation and subsequent peritonitis. The incidence of mesenteric vasculitis in patients with systemic lupus erythematosus is reported to be in range of 0.2–53%. A variety of symptoms have been observed in patients presenting with underlying autoimmune process however acute abdominal pain remains to be the most common presenting feature with reported frequencies of 33–62%. The cause of acute abdominal pain can be secondary to involvement of central nervous system, serositis, enteritis, pancreatitis, uraemia and primary peritonitis however mesenteric vasculitis leading to bowel ischemia remains to be the most serious.1,2,4 Computed Tomography (CT scan) remains to be the most valuable modality in early diagnosis of bowel ischemia. The strength of CT scan lies in its ability to demonstrate bowel wall and mesenteric vasculature simultaneously. Typically, CT findings in mesenteric ischemia include abnormal dilatation of loops with or without wall thickness (this can be focal or diffuse). Abnormal enhancement which are classically describe by double halo or target signs. Mesenteric oedema with prominent vasculature. Although these signs are sensitive in detection of bowel ischemia, the downside is their lack of specificity as they can be seen in a variety of other disease processes as well. Although intramural air is a classic finding in bowel ischemia due to thrombotic episode, it is rare in mesenteric vasculitis. The same was observed in our patients as well. Recent literature has also emphasized on the importance of initial mesenteric vascular prominence (Comb sign) as an early sign of mesenteric vasculitis. Similar picture was observed in one of our patients as well.3,5 Other finding seen on imaging in autoimmune processes as described in literature include lymphadenopathy, hepatosplenomegaly, inflammatory changes of the pancreas, ascites and renal parenchymal changes. Ascites and pancreatitis was observed as associated findings in our patients as well.3 According to findings of established literature patients usually respond well to high dose prednisolone therapy with resolution of symptoms. The same was observed in this series as well. A surgical intervention is rarely required. Most of the cases later need to be started on immunosuppressant therapy by use of agents like Azathioprine and Cyclophosphamide as relapse is common.2 The limitation of our series include lack of follow up scans to assess the extent of resolution of disease process on imaging. CONCLUSION Early diagnosis and management by high dose steroids is the key to prevent complications in cases of mesenteric vasculitis. The diagnosis should be considered in any patient with history of autoimmune disorder presenting with acute abdomen or having Imaging features of bowel Ischemia. REFERENCES 1. Sran S, Sran M, Patel N, Anand P. Lupus enteritis as an initial presentation of systemic lupus erythematosus. Case Rep Gastrointest Med 2014;2014:962735. 2. Tian XP, Zhang X. Gastrointestinal involvement in systemic lupus erythematosus: insight into pathogenesis, diagnosis and treatment. World J Gastroenterol 2010;16(24):2971–7. 3. Byun JY, Ha HK, Yu SY, Min JK, Park SH, Kim HY, et al. CT features of systemic lupus erythematosus in patients with acute abdominal pain: emphasis on ischemic bowel disease. Radiolog 1999;211(1):203–9. 4. Lee CK, Ahn MS, Lee EY, Shin JH, Cho YS, Ha HK, et al. Acute abdominal pain in systemic lupus erythematosus: focus on lupus enteritis (gastrointestinal vasculitis). Ann Rheum Dis 2002;61(6):547–50. 5. Wiesner W, Khurana B, Ji H, Ros PR. CT of acute bowel ischemia. Radiology 2003;226(3):635–50. Received: 14 August, 2015 Revised: 17 May,2016 Accepted: 26 December, 2016 Address for Correspondence: Dr. Saad Siddiqui, Department of Radiology, The Aga Khan University, Karachi- Pakistan Cell: +92 321 906 3099 Email: saadsiddiqui.5@gmail.com