1.Cap-assisted ERCP in Surgically Altered Anatomy.
Eun Seo PARK ; Tae Hoon LEE ; Sang Heum PARK ; Gyu Bong KO ; Bum Suk SON ; Yun Suk SHIM ; Sae Hwan LEE ; Hong Soo KIM ; Sun Joo KIM
Korean Journal of Gastrointestinal Endoscopy 2010;41(6):344-349
BACKGROUND/AIMS: Endoscopic retrograde cholangiopancreatography (ERCP) is a difficult procedure to perform on patients who have undergone a Billroth II gastrectomy, Whipple's operation or Roux-en-Y gastrobypass surgery. Our study was designed to evaluate the clinical usefulness of cap-assisted ERCP for beginner endoscopists in cases of surgically altered anatomy. METHODS: From April 2008 to March 2010, 16 patients with biliary diseases and who had previously undergone abdominal surgery such as Billroth II gastrectomy or Roux-en-Y operation were analyzed. A single endoscopist performed all the procedures using a cap-assisted gastroscope, after ERCP training. RESULTS: Cap-assisted ERCP was attempted in 24 sessions of 16 patients. Afferent loop intubation and selective bile duct cannulation was successfully achieved in 19 sessions (79.1%). Among the patients who had undergone a Billroth II gastrectomy, 19 out of 20 sessions were successfully conducted. Only 4 patients who had undergone a previous Roux-en-Y operation failed afferent loop intubation. Duodenal free wall perforation developed in one case. There were no cases of mortality. CONCLUSIONS: Therapeutic cap-assisted ERCP was useful in patients who had previously undergone a Billroth II gastrectomy and this may be helpful for inexperienced endoscopists.
Anastomosis, Roux-en-Y
;
Bile Ducts
;
Catheterization
;
Cholangiopancreatography, Endoscopic Retrograde
;
Gastrectomy
;
Gastroenterostomy
;
Gastroscopes
;
Humans
;
Intubation
2.A Case of Lymphangiomatosis Arising in the Colon.
Bum Suk SON ; Chang Kyun LEE ; Duk Su KIM ; Yong Sub LEE ; Suck Ho LEE ; Il Kwun CHUNG ; Sun Joo KIM ; Ji Hye LEE
Korean Journal of Gastrointestinal Endoscopy 2009;39(3):172-175
Lymphangioma is a benign vascular lesion that shows the characteristics of subepithelial tumor, which can proliferate in the lymphatic system. Only a few cases of multiple lymphangimas of the colon, the so called "colonic lymphanigomatosis", have been currently reported on the medical literature. Because lymphangioma is absolutely a benign tumor, it does not require any specific treatment, except for rare disease-related symptoms or complications such as anemia, intussusception and protein-losing enteropathy. Endoscopic resection for this tumor has sometimes been performed for both diagnostic and therapeutic purposes. We recently experienced a case of multiple colonic lymphangomas that arose in the ascending colon of a 46-year-old male patient and these lesions were found during performance of colonoscopy. The final diagnosis was confirmed by a pathologic examination of the specimen that was obtained via endoscopic resection. Follow-up colonoscopy at 1 year after the initial examination showed complete resolution of the previously noted lesions without any specific treatment. We report here on a very rare case of colonic lymphangiomatosis along with a brief review of the relevant literature.
Anemia
;
Colon
;
Colon, Ascending
;
Colonoscopy
;
Follow-Up Studies
;
Humans
;
Intestine, Large
;
Intussusception
;
Lymphangioma
;
Lymphatic System
;
Male
;
Middle Aged
;
Protein-Losing Enteropathies
3.A Case of Liposarcoma Arising in the Mesentery.
Bum Suk SON ; Su Jin SEOK ; Seung Kyu CHUNG ; Joon Seong LEE ; Moon Sung LEE ; Chan Sup SHIM ; Kyung Yul HUR ; So Young JIN
The Korean Journal of Gastroenterology 2009;54(4):243-247
A liposarcoma is the most common soft tissue sarcoma in adults with an incidence of about 20% of all soft tissue sarcomas. Although incidence differs from a region of origination, a case arisen from mesentery has rarely been reported. We experienced a case of liposarcoma arising from the mesentery of a 51-year-old male patient. He was treated by wide excision. Histologically, the tumor was composed of a mixed well-differentiated liposarcoma with myxoid and spindle cell type.
Diagnosis, Differential
;
Fluorodeoxyglucose F18/diagnostic use
;
Humans
;
Liposarcoma/*diagnosis/pathology/surgery
;
Magnetic Resonance Imaging
;
Male
;
Mesentery/*pathology
;
Middle Aged
;
Tomography, X-Ray Computed
4.A Case of Iliopsoas Abscess Complicating Active Crohn's Disease during Infliximab Induction Treatment.
Seung Kyu CHUNG ; Chang Kyun LEE ; Kyoung Hwan LEE ; Bum Suk SON ; Duk Su KIM ; Sun Joo KIM ; Kil Ho KANG
Intestinal Research 2009;7(2):118-122
Psoas abscesses are rare clinical entities complicating Crohn's disease (CD). However, psoas abscesses can cause poor outcomes because the diagnosis is frequently delayed due to the non-specific clinical features. Recently, we managed a case of a huge iliopsoas abscess in a 21-year-old man with a 4-year history of CD who presented with a limping gait and flexion contractures of the sacroiliac joint. Notably, the iliopsoas abscess developed during induction treatment with infliximab. The patient was successfully treated with antibiotics, surgical drainage, and a right hemicolectomy. Herein we present the case with a brief review of the literature.
Anti-Bacterial Agents
;
Antibodies, Monoclonal
;
Contracture
;
Crohn Disease
;
Drainage
;
Gait
;
Humans
;
Infliximab
;
Psoas Abscess
;
Sacroiliac Joint
;
Young Adult
5.A Case of Iliopsoas Abscess Complicating Active Crohn's Disease during Infliximab Induction Treatment.
Seung Kyu CHUNG ; Chang Kyun LEE ; Kyoung Hwan LEE ; Bum Suk SON ; Duk Su KIM ; Sun Joo KIM ; Kil Ho KANG
Intestinal Research 2009;7(2):118-122
Psoas abscesses are rare clinical entities complicating Crohn's disease (CD). However, psoas abscesses can cause poor outcomes because the diagnosis is frequently delayed due to the non-specific clinical features. Recently, we managed a case of a huge iliopsoas abscess in a 21-year-old man with a 4-year history of CD who presented with a limping gait and flexion contractures of the sacroiliac joint. Notably, the iliopsoas abscess developed during induction treatment with infliximab. The patient was successfully treated with antibiotics, surgical drainage, and a right hemicolectomy. Herein we present the case with a brief review of the literature.
Anti-Bacterial Agents
;
Antibodies, Monoclonal
;
Contracture
;
Crohn Disease
;
Drainage
;
Gait
;
Humans
;
Infliximab
;
Psoas Abscess
;
Sacroiliac Joint
;
Young Adult
6.Five Cases of Phytophotodermatitis Caused by Fig Leaves and Relevant Literature Review.
Jin Hwa SON ; Hyunju JIN ; Hyang Suk YOU ; Woo Haing SHIM ; Jeong Min KIM ; Gun Wook KIM ; Hoon Soo KIM ; Hyun Chang KO ; Moon Bum KIM ; Byung Soo KIM
Annals of Dermatology 2017;29(1):86-90
Phytophotodermatitis is a condition caused by sequential exposure to photosensitizing substances present in plants followed by ultraviolet light. Several plants (e.g., limes, celery, fig, and wild parsnip) contain furocoumarin compounds (psoralens). It is important for dermatologists to be aware of phytophotodermatitis because it may be misdiagnosed as cellulitis, tinea, or allergic contact dermatitis. We present five patients with a sharply defined erythematous swollen patch with bullae on both feet. They described soaking their feet in a fig leaves decoction to treat their underlying dermatologic diseases. Within 24 hours, all patients had a burning sensation in their feet, and erythema and edema had developed on the feet dorsa with exception of the portion of the skin covered by the sandals. Histopathologic examinations revealed sub-epithelial blisters with intensive epidermal necrosis. Phytophotodermatitis was ultimately diagnosed and, after several days, the patients' skin lesions began to recover upon treatment with systemic and topical corticosteroids. Unfortunately, since there are no studies providing sufficient evidence on the benefits of fig leaves, they should be used with caution.
Adrenal Cortex Hormones
;
Apium graveolens
;
Blister
;
Burns
;
Cellulitis
;
Citrus aurantiifolia
;
Dermatitis, Allergic Contact
;
Edema
;
Erythema
;
Ficus
;
Foot
;
Humans
;
Necrosis
;
Photosensitivity Disorders
;
Sensation
;
Skin
;
Tinea
;
Ultraviolet Rays
7.Five Cases of Phytophotodermatitis Caused by Fig Leaves and Relevant Literature Review.
Jin Hwa SON ; Hyunju JIN ; Hyang Suk YOU ; Woo Haing SHIM ; Jeong Min KIM ; Gun Wook KIM ; Hoon Soo KIM ; Hyun Chang KO ; Moon Bum KIM ; Byung Soo KIM
Annals of Dermatology 2017;29(1):86-90
Phytophotodermatitis is a condition caused by sequential exposure to photosensitizing substances present in plants followed by ultraviolet light. Several plants (e.g., limes, celery, fig, and wild parsnip) contain furocoumarin compounds (psoralens). It is important for dermatologists to be aware of phytophotodermatitis because it may be misdiagnosed as cellulitis, tinea, or allergic contact dermatitis. We present five patients with a sharply defined erythematous swollen patch with bullae on both feet. They described soaking their feet in a fig leaves decoction to treat their underlying dermatologic diseases. Within 24 hours, all patients had a burning sensation in their feet, and erythema and edema had developed on the feet dorsa with exception of the portion of the skin covered by the sandals. Histopathologic examinations revealed sub-epithelial blisters with intensive epidermal necrosis. Phytophotodermatitis was ultimately diagnosed and, after several days, the patients' skin lesions began to recover upon treatment with systemic and topical corticosteroids. Unfortunately, since there are no studies providing sufficient evidence on the benefits of fig leaves, they should be used with caution.
Adrenal Cortex Hormones
;
Apium graveolens
;
Blister
;
Burns
;
Cellulitis
;
Citrus aurantiifolia
;
Dermatitis, Allergic Contact
;
Edema
;
Erythema
;
Ficus
;
Foot
;
Humans
;
Necrosis
;
Photosensitivity Disorders
;
Sensation
;
Skin
;
Tinea
;
Ultraviolet Rays
8.Rectal Endometriosis That Is Difficult to Differentiate from Endoscopically Resectable Subepitherial Lesion.
Seung Kyu CHUNG ; Suck Ho LEE ; Bum Suk SON ; Chang Kyun LEE ; Tae Hoon LEE ; Il Kwun CHUNG ; Sun Joo KIM ; Ji Hye LEE
Korean Journal of Gastrointestinal Endoscopy 2010;41(5):319-323
Endometriosis occurs most frequently in the intestine. In the pelvic organs intestinal endometriosis presents with various symptoms and endoscopic findings. If an asymptomatic submucosal lesion is found in the sigmoid colon or rectum of reproductive women, a differential diagnosis should be done. Owing to advancements in endoscopic therapy, endoscopic excision has been attempted for various subepithelial lesions. To successfully do an endoscopic excision, accurate diagnosis should be obtained through diagnostic tests such as endoscopic ultrasonography prior to excision. Here the authors report a case of rectal endometriosis in an asymptomatic woman of reproductive age. They attempted endoscopic resection based on the endoscopic finding that the subepithelial lesion was limited to the submucosal layer in endoscopic ultrasonography. This conclusion turned out to be a mistaken one. Because of tumor adhesion to the proper muscular layer, we failed to successfully conduct an endoscopic excision. Ultimately, we did surgery and diagnosed rectal endometriosis.
Colon, Sigmoid
;
Diagnosis, Differential
;
Diagnostic Tests, Routine
;
Endometriosis
;
Endosonography
;
Female
;
Humans
;
Intestines
;
Rectum
9.Successful Bile Duct Cannulation Guided by Indigocarmine Injection via PTGBD.
Bum Suk SON ; Sang Heum PARK ; Tae Hoon LEE ; Seung Kyu CHUNG ; Jae Man PARK ; Il Kwun CHUNG ; Hong Soo KIM ; Sun Joo KIM
Korean Journal of Gastrointestinal Endoscopy 2011;42(1):62-66
Even though percutaneous transhepatic gallbladder drainage (PTGBD) is performed prior to ERCP or following ERCP because of the patients' medical condition or failed bile duct cannulation, there are no definite endoscopic landmarks that are useful for successful bile duct cannulation in some cases. We report here on 4 patients in whom selective bile duct cannulation, as guided by the endoscopic landmarks, was successful following indigocarmine injection via PTGBD.
Bile
;
Bile Ducts
;
Catheterization
;
Cholangiopancreatography, Endoscopic Retrograde
;
Drainage
;
Gallbladder
;
Humans
10.A Case of Alstrom Syndrome.
Kun Ho YOON ; Ho Young SON ; Sung Koo KANG ; Yoon Hee CHOI ; Bong Yeon CHA ; Hwan Suk CHO ; Ki Bum KIM ; Ji Ho KANG ; Young Mi CHOO ; Sang Soo BAE
Journal of Korean Society of Endocrinology 1998;13(3):501-508
The Alstrom syndrome is inherited autosomal recessive disorder, characterized by obesity, diabetes mellitus, pigmentary retinal degeneration, normal intelligence, sensorineural hearing loss, baldness, acanthosis nigricans, male hypogonadism, hyperuricemia and hypertriglyceridemia. There is no reported case of Alstrom syndrome in Korea yet. We experienced a 29-year-old female patient with clinical characteristics similar to Alstrom syndrome who was admitted due to poorly controlled diabetes mellitus and diabetic retinopathy with hemorrhage. We report this case with the review of literatures.
Acanthosis Nigricans
;
Adult
;
Alopecia
;
Alstrom Syndrome*
;
Diabetes Mellitus
;
Diabetic Retinopathy
;
Female
;
Hearing Loss, Sensorineural
;
Hemorrhage
;
Humans
;
Hypertriglyceridemia
;
Hyperuricemia
;
Hypogonadism
;
Intelligence
;
Korea
;
Male
;
Obesity
;
Retinal Degeneration