1.A Case of Splenic Pseudocyst Difficult to Differentiate from Splenic Lymphangioma.
Shin Ae LEE ; Sang Young HAN ; Eun Joo LEE ; Byung Pyo KWON ; In Young KOH ; Hae Jong CHOI ; Min Chan KIM ; Jin Han CHO
The Korean Journal of Gastroenterology 2006;48(6):427-430
Splenic pseudocyst is a rare complication of abdominal trauma. Although it is rare, splenic pseudocyst is well-documented in the literature. According to the current classification, approximately 30% of all splenic cysts or pseudocysts result from direct abdominal trauma. In addition, chronic pancreatitis leads to change of nearby organs with possible acute and chronic complications including splenic lesions. This unusual complication can occur in both emergent and nonemergent conditions. The useful diagnostic procedures to assess intrasplenic pseudocyst are sonogram, CT scan, splenic scan, and occasionally angiography. However, definite diagnosis of pseudocyst is possible only after splenectomy when the absence of epithelial lining is confirmed histologically. Splenic pseudocyst requires surgical resection. We experienced a 31-year-old man who confirmed of warmness in the left side of back with left upper quadrant abdominal pain for several months. First impression was splenic lymphangioma based on CT scan and sonogram finding. Splenectomy was performed. Microscopic examination revealed splenic pseudocyst with fibrous capsule without epithelial lining.
Adult
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Cysts/*diagnosis/radiography/ultrasonography
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Diagnosis, Differential
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Humans
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Lymphangioma/diagnosis
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Male
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Splenectomy
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Splenic Diseases/*diagnosis/radiography/ultrasonography
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Splenic Neoplasms/diagnosis
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Tomography, X-Ray Computed
2.Gastrointestinal stromal tumor with synchronous isolated parenchymal splenic metastasis of ovarian cancer.
Wei LI ; Xin WU ; Ning WANG ; Duo YIN ; Shu-Lan ZHANG
Chinese Medical Journal 2011;124(24):4372-4375
Gastrointestinal stromal tumor (GIST) represents the most common intramural mesenchymal tumor of the gastrointestinal tract, but the synchronous occurrence of GIST in the stomach and gynecological cancer is rare. We present a unique case of a 56-year-old female patient who was diagnosed with the synchronous development of GIST and an isolated parenchymal splenic metastasis of ovarian cancer. She underwent a wide local excision of gastric lesions with splenectomy. A morphological (histological and immunohistochemical) study established a spindle-cell type of gastrointestinal tumor that expressed CD117, and a parenchymal recurrence of ovarian papillary serous adenocarcinoma. The patient has remained alive and disease-free for 30 months since the last operation. A small GIST concomitant with an isolated parenchymal splenic metastasis of ovarian cancer is rarely encountered. The coexistence of GIST with other malignancies constitutes an intriguing oncologic model. Surgeons are advised to be alert against possible primary GIST accompanying other neoplasms.
Female
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Gastrointestinal Stromal Tumors
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diagnostic imaging
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secondary
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Humans
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Middle Aged
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Ovarian Neoplasms
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complications
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Radiography
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Splenic Neoplasms
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secondary
3.CT and MRI Findings of Sclerosing Angiomatoid Nodular Transformation of the Spleen: Spoke Wheel Pattern.
Devrim A KARAOSMANOGLU ; Musturay KARCAALTINCABA ; Deniz AKATA
Korean Journal of Radiology 2008;9(Suppl):S52-S55
Sclerosing angiomatoid nodular transformation of the spleen is a recently described benign pathologic entity that is characterized by round shaped vascular spaces that are lined by endothelial cells, and the spaces are circumscribed by granulomatoid structures. Microscopically, all the reported cases had multiple angiomatoid nodules in a fibrosclerotic stroma. Each angiomatoid nodule was made up of slit-like, round or irregular shaped vascular spaces that were lined by endothelial cells and interspersed ovoid cells. We present here the CT and dynamic gadolinium-enhanced MR findings of a patient with sclerosing angiomatoid nodular transformation. The spoke-wheel pattern that was observed on MRI in this case may be an important imaging clue for making the correct diagnosis of this benign lesion.
Adult
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Cell Transformation, Neoplastic/pathology
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Gadolinium/diagnostic use
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Histiocytoma, Benign Fibrous/*pathology/*radiography
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Humans
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*Magnetic Resonance Imaging
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Male
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Splenic Neoplasms/*pathology/*radiography
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*Tomography, X-Ray Computed
4.Hepatosplenic B-cell lymphoma associated with hemophagocytic syndrome: a case report.
Sang Yong KWON ; Je Jung LEE ; Ik Joo CHUNG ; Hyeoung Joon KIM ; Moo Rim PARK ; Hyung Seok KIM ; Chang Soo PARK
Journal of Korean Medical Science 1999;14(6):671-674
While T-cell non-Hodgkin's lymphoma (NHL) associated with hemophagocytic syndrome (HPS) has been frequently observed, B-cell NHL associated with HPS has been rarely reported. We report a case of hepatosplenic B-cell lymphoma associated with HPS in a 41-year-old woman who presented with fever of unknown origin. An abdominal CT scan revealed splenomegaly with focal splenic infarction. Splenectomy and a liver wedge biopsy showed sinusoidal-pattern infiltration of medium to large tumor cells with positive reaction to a B-lymphocyte marker. Findings on bone marrow examination showed proliferation of histiocytes with avid hemophagocytosis.
Adult
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Antigens, CD/analysis
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Antineoplastic Agents, Combined/therapeutic use
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Bone Marrow Cells/pathology
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Case Report
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Female
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Histiocytosis, Non-Langerhans-Cell/pathology
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Histiocytosis, Non-Langerhans-Cell/complications*
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Human
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Liver Neoplasms/radiography
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Liver Neoplasms/pathology
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Liver Neoplasms/complications*
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Lymphoma, B-Cell/radiography
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Lymphoma, B-Cell/pathology
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Lymphoma, B-Cell/complications*
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Splenic Neoplasms/radiography
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Splenic Neoplasms/pathology
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Splenic Neoplasms/complications*
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Splenomegaly/radiography
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Tomography, X-Ray Computed
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Tumor Markers, Biological/analysis
5.Two Cases of Portal Annular Pancreas.
Ji Young JANG ; Young Eun CHUNG ; Chang Moo KANG ; Sung Hoon CHOI ; Ho Kyoung HWANG ; Woo Jung LEE
The Korean Journal of Gastroenterology 2012;60(1):52-55
Portal annular pancreas is one of the pancreatic fusion anomalies in which the uncinate process of the pancreas extends to fuse with the dorsal pancreas by encircling the portal vein or superior mesenteric vein. We report two consecutive patients with portal annular pancreas. The first case is a 71-year-old male patient who underwent a pancreaticoduodenectomy for intraductal papillary mucinous neoplasm in the head of pancreas. His preoperative computed tomography scan showed the suprasplenic type portal annular pancreas. The second case is a 74-year-old female patient who underwent a laparoscopic anterior radical antegrade modular pancreatosplenectomy (RAMPS) for pancreatic body cancer. In operative finding, portal confluence (superior mesenteric vein-splenic vein-portal vein) was encased with the uncinate process of pancreas in both cases. Therefore, they required pancreatic division at the pancreatic neck portion twice. During the postoperative period, grade B and A, respectively, postoperative pancreatic fistulas occurred and were controlled by conservative management. Surgeons need to know about this rare pancreatic condition prior to surgical intervention to avoid complications, and to provide patients with well-designed, case-specific pancreatic surgery.
Adenocarcinoma, Mucinous/diagnosis/surgery
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Aged
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Female
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Humans
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Male
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Mesenteric Veins/radiography
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Pancreas/abnormalities
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Pancreatic Diseases/*diagnosis/therapy
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Pancreatic Fistula/etiology
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Pancreatic Neoplasms/diagnosis/surgery
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Pancreaticoduodenectomy/adverse effects
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Portal Vein/radiography
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Splenic Vein/radiography
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Tomography, X-Ray Computed
6.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
7.An insulinoma with an aberrant feeder from the splenic artery detected by super-selective arterial calcium stimulation with venous sampling.
Joon Ho MOON ; Eun Ky KIM ; Ah Reum KHANG ; Hyo Cheol KIM ; Jin Young JANG ; Young Min CHO
The Korean Journal of Internal Medicine 2015;30(1):118-121
No abstract available.
Biopsy
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Blood Glucose/metabolism
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C-Peptide/blood
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Calcium Gluconate/administration & dosage/*diagnostic use
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Female
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Humans
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Immunohistochemistry
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Injections, Intra-Arterial
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Insulin/blood
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Insulinoma/blood/*blood supply/pathology/surgery
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Middle Aged
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Pancreatic Neoplasms/blood/*blood supply/pathology/surgery
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Pancreaticoduodenectomy
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Splenic Artery/*radiography
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*Tomography, X-Ray Computed
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Treatment Outcome
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Tumor Markers, Biological/blood