1.Abdominal Epilepsy and Foreign Body in the Abdomen - Dilemma in Diagnosis of Abdominal Pain.
Noor TOPNO ; Mahesh S GOPASETTY ; Annappa KUDVA ; B LOKESH
Yonsei Medical Journal 2005;46(6):870-873
There are many medical causes of abdominal pain; abdominal epilepsy is one of the rarer causes. It is a form of temporal lobe epilepsy presenting with abdominal aura. Temporal lobe epilepsy is often idiopathic, however it may be associated with mesial temporal lobe sclerosis, dysembryoplastic neuroepithelial tumors and other benign tumors, arterio-venous malformations, gliomas, neuronal migration defects or gliotic damage as a result of encephalitis. When associated with anatomical abnormality, abdominal epilepsy is difficult to control with medication alone. In such cases, appropriate neurosurgery can provide a cure or, at least, make this condition easier to treat with medication. Once all known intra-abdominal causes have been ruled out, many cases of abdominal pain are dubbed as functional. If clinicians are not aware of abdominal epilepsy, this diagnosis is easily missed, resulting in inappropriate treatment. We present a case report of a middle aged woman presenting with abdominal pain and episodes of unconsciousness. On evaluation she was found to have an intra-abdominal foreign body (needle). Nevertheless, the presence of this entity was insufficient to explain her episodes of unconsciousness. On detailed analysis of her medical history and after appropriate investigations, she was diagnosed with temporal lobe epilepsy which was treated with appropriate medications, and which resulted in her pain being relieved.
Radiography, Abdominal
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Humans
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Foreign Bodies/pathology/*radiography
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Female
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Epilepsy, Temporal Lobe/*diagnosis/drug therapy
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Electroencephalography
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Anticonvulsants/therapeutic use
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Adult
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Abdominal Pain/drug therapy/*etiology/*radiography
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*Abdomen
2.Follicular Dendritic Cell Sarcoma of the Abdomen: the Imaging Findings.
Tae Wook KANG ; Soon Jin LEE ; Hye Jong SONG
Korean Journal of Radiology 2010;11(2):239-243
Follicular dendritic cell sarcoma is a rare neoplasm that originates from follicular dendritic cells in lymphoid follicles. This disease usually involves the lymph nodes, and especially the head and neck area. Rarely, extranodal sites may be affected, including tonsil, the oral cavity, liver, spleen and the gastrointestinal tract. We report here on the imaging findings of follicular dendritic cell sarcoma of the abdomen that involved the retroperitoneal lymph nodes and colon. It shows as a well-defined, enhancing homogenous mass with internal necrosis and regional lymphadenopathy.
Abdomen/ultrasonography
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Abdominal Neoplasms/complications/*radiography/*ultrasonography
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Abdominal Pain/etiology
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Aged
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Colon/radiography/ultrasonography
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Colonic Neoplasms/complications/*radiography/*ultrasonography
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Dendritic Cell Sarcoma, Follicular/complications/*radiography/*ultrasonography
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Dendritic Cells, Follicular/radiography/ultrasonography
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Diagnosis, Differential
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Dyspepsia/etiology
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Female
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Gastrointestinal Hemorrhage/etiology
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Humans
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Lymph Nodes
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Male
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Middle Aged
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Radiography, Abdominal/methods
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Retroperitoneal Space/radiography/ultrasonography
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Tomography, X-Ray Computed/methods
3.Clinical and Radiologic Review of Uncommon Cause of Profound Iron Deficiency Anemia: Median Arcuate Ligament Syndrome.
Yasemin GUNDUZ ; Kiyasettin ASIL ; Yakup Ersel AKSOY ; Lacin TATLI AYHAN
Korean Journal of Radiology 2014;15(4):439-442
Median arcuate ligament syndrome is an anatomic and clinical entity characterized by dynamic compression of the proximal celiac artery by the median arcuate ligament, which leads to postprandial epigastric pain, vomiting, and weight loss. These symptoms are usually nonspecific and are easily misdiagnosed as functional dyspepsia, peptic ulcer disease, or gastropathy. In this report, we presented a 72-year-old male patient with celiac artery compression syndrome causing recurrent abdominal pain associated with gastric ulcer and iron deficiency anemia. This association is relatively uncommon and therefore not well determined. In addition, we reported the CT angiography findings and three-dimensional reconstructions of this rare case.
Abdominal Pain/*etiology
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Aged
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Anemia, Iron-Deficiency/*etiology
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Angiography/methods
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Arterial Occlusive Diseases/radiography
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Celiac Artery/*abnormalities/radiography
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Constriction, Pathologic/complications/*radiography
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Diaphragm
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Humans
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Male
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Recurrence
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Stomach Ulcer/complications/*radiography
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Syndrome
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Tomography, X-Ray Computed
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Weight Loss
4.Endovascular Stent Graft for Treatment of Complicated Spontaneous Dissection of Celiac Artery: Report of Two Cases.
Ung Rae KANG ; Young Hwan KIM ; Young Hwan LEE
Korean Journal of Radiology 2013;14(3):460-464
We report 2 cases of complicated spontaneous dissection of the celiac artery, which were successfully treated by a stent graft. The first patient was a 47-year-old man who presented with acute abdominal pain. CT scan showed ruptured saccular aneurysm with surrounding retroperitoneal hematoma. The second patient was a 57-year-old man with progressive dissecting aneurysm. Endovascular stent graft was placed in the celiac trunk to control bleeding, and to prevent rupture in each patient. Follow-up CT scans showed complete obliteration of a dissecting aneurysm.
Abdominal Pain/etiology/radiography
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Aneurysm, Dissecting/*therapy
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Aneurysm, Ruptured/prevention & control
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Celiac Artery/*injuries
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Hematoma/etiology/radiography
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Hemorrhage/etiology/radiography
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Humans
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Male
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Middle Aged
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Retroperitoneal Space
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Rupture, Spontaneous/therapy
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*Stents
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Tomography, X-Ray Computed/adverse effects
5.Strangulated Small Bowel Obstruction Following Endoscopic Retrograde Cholangiopancreatography.
Do Young KIM ; Yong Jin KIM ; Tae Yoon LEE ; Chan Sup SHIM ; Hyun Ah CHUNG ; In Sung SON ; Young Koog CHEON
The Korean Journal of Internal Medicine 2012;27(3):363-365
No abstract available.
Abdominal Pain/etiology
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Aged, 80 and over
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Cholangiopancreatography, Endoscopic Retrograde/*adverse effects
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Female
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Humans
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Ileal Diseases/etiology/radiography/surgery
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Intestinal Obstruction/*etiology/radiography/surgery
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Tomography, X-Ray Computed
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Treatment Outcome
6.Small Bowel Volvulus Induced by Mesenteric Lymphangioma in an Adult: a Case Report.
Jin Hee JANG ; Su Lim LEE ; Young Mi KU ; Chang Hyeok AN ; Eun Deok CHANG
Korean Journal of Radiology 2009;10(3):319-322
Mesenteric lymphangiomas are rare abdominal masses that are seldom associated with small bowel volvulus, and especially in adult patients. We report here on an unusual case of small bowel volvulus that was induced by a mesenteric lymphangioma in a 43-year-old man who suffered from repeated bouts of abdominal pain. At multidetector CT, we noticed whirling of the cystic mesenteric mass and the adjacent small bowel around the superior mesenteric artery. Small bowel volvulus induced by the rotation of the mesenteric lymphangioma was found on exploratory laparotomy. Lymphangioma should be considered as a rare cause of small bowel volvulus in adult patients.
Abdominal Pain/etiology
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Adult
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Contrast Media/diagnostic use
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Diagnosis, Differential
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Humans
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Intestinal Volvulus/*diagnosis/etiology/surgery
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Intestine, Small/*radiography/surgery
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Lymphangioma/*complications/surgery
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Male
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Mesenteric Artery, Superior/*radiography/surgery
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Radiographic Image Enhancement/methods
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Rare Diseases
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Tomography, X-Ray Computed
8.A Case of Henoch-Schonlein Purpura with Psoas Muscle Abscess and Full-blown Gastrointestinal Complications.
Hee Jung LEE ; Sun Moon KIM ; Sung Ro YUN ; Tae Hee LEE ; Euyi Hyeog IM ; Kyu Chan HUH ; Young Woo CHOI ; Young Woo KANG
The Korean Journal of Gastroenterology 2007;49(2):114-118
Henoch-Schonlein purpura (HSP) is a vasculitis involving small vessels of skin, joints, gastrointestinal (GI) tract, and kidneys. The patients typically show palpable purpura with one or more characteristic manifestations including abdominal pain, hematuria or arthritis. HSP shows gastrointestinal symptoms in 50~85% of patients, and in 14~40% of patients GI symptoms precede purpuric rash which makes the diagnosis of HSP difficult. We present a case of Henoch-Schonlein purpura with GI bleeding, septic shock by ileal microperforation, small bowel obstruction as a result of ileal stricture and psoas muscle abscess.
Abdominal Pain
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Anti-Inflammatory Agents/therapeutic use
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Colonoscopy
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Gastrointestinal Diseases/*diagnosis/etiology/pathology
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Gastrointestinal Hemorrhage/diagnosis
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Humans
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Male
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Middle Aged
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Prednisolone/therapeutic use
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Psoas Abscess/etiology/*radiography
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Purpura, Schoenlein-Henoch/*complications/*diagnosis/pathology
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Tomography, X-Ray Computed
9.Primary Extraskeletal Mesenchymal Chondrosarcoma Arising from the Pancreas.
Bae Geun OH ; Yoon Hee HAN ; Byung Hoon LEE ; Su Young KIM ; Yoon Joon HWANG ; Jung Wook SEO ; Yong Hoon KIM ; Soon Joo CHA ; Gham HUR ; Mee JOO
Korean Journal of Radiology 2007;8(6):541-544
We report here on a case of primary extraskeletal mesenchymal chondrosarcoma that arose from the pancreas. A 41-year-old man was evaluated by CT to find the cause of his abdominal pain. The CT scans showed a heterogeneously enhancing necrotic mass with numerous areas of coarse calcification, and this was located in the left side of the retroperitoneal space and involved the body and tail of the pancreas. Portal venography via the celiac axis also showed invasion of the splenic vein. Following excision of the mass, it was pathologically confirmed to be primary extraskeletal mesenchymal chondrosarcoma that arose from the pancreas.
Abdominal Pain/etiology
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Adult
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Chondrosarcoma, Mesenchymal/complications/*diagnosis/surgery
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Contrast Media/administration & dosage
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Diagnosis, Differential
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Humans
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Iohexol/analogs & derivatives/diagnostic use
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Male
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Necrosis
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Pancreas/pathology/radiography
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Pancreatic Neoplasms/complications/*diagnosis/surgery
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Portal Vein/radiography
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Radiographic Image Enhancement/methods
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Rare Diseases
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Retroperitoneal Space/radiography
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Splenic Vein/radiography
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Tomography, X-Ray Computed/methods
10.Presumed dapsone-induced drug hypersensitivity syndrome causing reversible hypersensitivity myocarditis and thyrotoxicosis.
Rachael Y L TEO ; Yong-Kwang TAY ; Chong-Hiok TAN ; Victor NG ; Daniel C T OH
Annals of the Academy of Medicine, Singapore 2006;35(11):833-836
INTRODUCTIONA 22-year-old Malay soldier developed dapsone hypersensitivity syndrome 12 weeks after taking maloprim (dapsone 100 mg/pyrimethamine 12.5 mg) for anti-malarial prophylaxis.
CLINICAL PICTUREHe presented with fever, rash, lymphadenopathy and multiple-organ involvement including serositis, hepatitis and thyroiditis. Subsequently, he developed congestive heart failure with a reduction in ejection fraction on echocardiogram, and serum cardiac enzyme elevation consistent with a hypersensitivity myocarditis.
TREATMENTMaloprim was discontinued and he was treated with steroids, diuretics and an angiotensin-converting-enzyme inhibitor.
OUTCOMEHe has made a complete recovery with resolution of thyroiditis and a return to normal ejection fraction 10 months after admission.
CONCLUSIONIn summary, we report a case of dapsone hypersensitivity syndrome with classical symptoms of fever, rash and multi-organ involvement including a rare manifestation of myocarditis. To our knowledge, this is the first case of dapsone-related hypersensitivity myocarditis not diagnosed in a post-mortem setting. As maloprim is widely used for malaria prophylaxis, clinicians need to be aware of this unusual but potentially serious association.
Abdominal Pain ; drug therapy ; Adult ; Anti-Inflammatory Agents, Non-Steroidal ; adverse effects ; therapeutic use ; Biopsy ; Dapsone ; adverse effects ; therapeutic use ; Diagnosis, Differential ; Drug Hypersensitivity ; complications ; pathology ; Echocardiography ; Electrocardiography, Ambulatory ; Fever ; drug therapy ; Follow-Up Studies ; Humans ; Male ; Myocarditis ; diagnosis ; etiology ; Radiography, Thoracic ; Skin ; pathology ; Thyrotoxicosis ; diagnosis ; etiology