ABSTRACT
Biliary papillomatosis is a rare disease with a high risk of recurrence and malignant transformation. Therapeutic options include partial hepatectomy, Whipple's procedure and liver transplantation. If there is no surgical option left due to several reasons, local palliative procedures such as biliary stenting and drainage for the treatment of cholestasis are considered, but tumor growth cannot be influenced. Photodynamic therapy might be a new additional, palliative option for patients with biliary papillomatosis who are not eligible for surgery. Benign biliary stricture is a rare complication of photodynamic therapy. We report here a case of a 63-year-old male who developed benign biliary stricture after photodynamic therapy using the photosensitizer photofrin.
Subject(s)
Humans , Male , Middle Aged , Cholestasis , Constriction, Pathologic , Dihematoporphyrin Ether , Drainage , Hepatectomy , Liver Transplantation , Papilloma , Photochemotherapy , Rare Diseases , Recurrence , StentsABSTRACT
A papilomatose das vias biliares (PVB) é uma afecção rara, descrita inicialmente por Caroli, em 1959. Até o ano de 2001, apenas cerca de 50 casos foram descritos na literatura mundial. O diagnóstico da PVB dificilmente é realizado no pré-operatório, pois os achados de exames de imagem e endoscópicos quase sempre são inespecíficos, e muitas vezes apenas sugerem o diagnóstico de neoplasia das vias biliares. O objetivo da presente publicação é relatar um caso de PVB tratado por hepatectomia esquerda com o diagnóstico provável de colangiocarcinoma da confluência dos hepáticos. O diagnóstico definitivo de PVB só foi estabelecido após estudo anatomopatológico da peça cirúrgica. São comentados aspectos relacionados ao diagnóstico diferencial, às opões de tratamento propostas para a PVB, bem como o prognóstico dos pacientes submetidos à ressecção.
Biliary papillomatosis (BP) is a rare disease, initially described for Caroli, in 1959. Until the year of 2001, only about 50 cases had been described in world-wide literature. The diagnosis of the BP hardly is carried through in pre-operatory, therefore the findings of image examinations and endoscopies almost always are not specifics, and many times only suggest diagnosis of neoplasia of biliary ducts. The objective of present publication is to relate a case of BP treated for left hepatectomy with probable diagnosis of cholangiocarcionoma of hepatics ducts confluence. Definitive diagnosis of BP alone was established after anatomopathological study of surgical specimen. Aspects related to differential diagnosis, treatment options proposals for the BP, as well as prognostic of the patients submitted to surgery are commented.
Subject(s)
Male , Female , Bile Ducts/pathology , Hepatectomy , Jaundice, Obstructive/surgery , Jaundice, Obstructive/etiology , Jaundice, Obstructive/pathology , Papillomaviridae/pathogenicity , Diagnosis, Differential , Diagnostic Imaging , PrognosisABSTRACT
Objective To investigate the diagnosis and treatment for biliary papillomatosis. Methods 23 patients who were pathologically diagnosed as biliary papillomatosis and treated in our hospital from Jan. 2003 to Mar. 2008 were enrolled in this study. Their ages, genders, clinical manifestations, diagnostic approaches,histopathological findings, intraoperative findings, treatments and prognosis were analyzed retrospectively. Recal manifestations were abdominal pain (83.3%) and obstructive jaundice (72.2%). All the patients were diagnosed pathologically through intraoperative frozen section. No patient was diagnosed preoperatively. Anatomically, solitary lesion was observed in 10 patients (43.5%) and multiple lesions in 13 patients (56.5%), with a median tumor size of 2.6 cm. Microscopically, carcinomatous change was found in one patient, mild atypical hyperplasia in three, and medium atypical hyperplasia in one. Therapies mainly included radical excision and palliative external drainage. All but one patient recovered well postoperatively. This patient had anastomotic leak. All 23 patients were followed up with a mean period of 34 months. During the follow-up, three patients died as a consequence of biliary malignancy, one patient had the recurrence and others without recurrence. Conclusions Biliary papillomatosis is very difficult to diagnose preoperatively and the definitive diagnosis mainly depends on intraoperative and postoperative pathologic examination. To obtain a better prognosis, management should be aimed at radical excision. Intraoperative cholangioscopic evaluation and frozen section are strongly recommended to guide the choice of appropriate therapeutic approach.
ABSTRACT
Photodynamic therapy has been widely used in the treatment of various cancerous diseases. However, photodynamic therapy with a photosensitizer can cause a photosensitivity reaction on the skin. We report a case of a 64-year-old woman diagnosed with photosensitivity reaction after photodynamic therapy using the photosensitizer, porfimer. She presented to the emergency room with a skin rash on her face, neck, and both upper and lower extremities nine days after the photodynamic therapy. She denied any outdoor activity during that period. After administration of systemic corticosteroid and anti-histamine, her skin lesions resolved completely within seven days.
Subject(s)
Female , Humans , Middle Aged , Dihematoporphyrin Ether , Emergencies , Exanthema , Lower Extremity , Neck , Papilloma , Photochemotherapy , SkinABSTRACT
Biliary papillomatosis is a rare disease entity characterized by multiple papillary adenomas along the bile duct mucosa. It is widely accepted that the adenoma-carcinoma sequence represents the process by which most, if not all, cholangiocarcinomas of an intraductal-growing type arise. Interestingly, friable papillary projections easily detached from the primary site can be implanted into the other sites in the bile duct in suitable animal models, resulting in multiple tumors. A 76-year-old male was referred to our hospital due to intermittent abdominal discomfort. Imaging workups revealed two lesions: wall thickening in the proximal portion of the left interhepatic duct and abrupt narrowing of the distal common bile duct. A hepatopancreaticoduodenectomy was carried out and pathological analysis demonstrated a well-differentiated adenocarcinoma of the left hepatic duct and carcinoma in situ of the distal common bile duct on a background of biliary papillomatosis. Six days after the operation, the patient received a re-exploration due to ruptured mesenteric vessels. Unfortunately, 3 months after the initial operation, the patient died of aspiration pneumonia. Biliary papillomatosis can present with a broad spectrum of disease characteristics ranging from adenoma to, usually, low-grade adenocarcinoma. If there is a complete excision, and a favorable postoperative course is secured, excellent survival can be expected after surgery.
Subject(s)
Aged , Humans , Male , Adenocarcinoma , Adenoma , Bile Ducts , Carcinoma in Situ , Cholangiocarcinoma , Common Bile Duct , Hepatic Duct, Common , Models, Animal , Mucous Membrane , Papilloma , Pneumonia, Aspiration , Rare DiseasesABSTRACT
The mucin-hypersecreting biliary papillomatosis is a premalignant neoplasm characterized by intraductal papillary proliferation involving extensive areas of the intrahepatic and/or extrahepatic bile duct. We report a case of mucin-hypersecreting biliary papillomatosis manifested as obstructive jaundice and diagnosed only by microscopy, with a review of literatures. A 74-year-old female, who had a past history of cholecystectomy about 13 years ago, was admitted to our hospital with jaundice. A CT scan showed marked dilatation of intrahepatic and extrahepatic bile duct without intraductal filling defect or extrabiliary mass. During endoscopic retrograde cholangiopancreatography, mucin extrusion from the duodenal major papilla and dilated common bile duct with amorphous filling defects was noted. Percutaneous transhepatic biliary drainage for cholangioscopy was failed. In the operation field, there was a lot of mucin but was no visible mass at the common bile duct with bare eyes and cholangioscopy. However, papilloma was detected at the random biopsy specimen by microscopy. The patient underwent partial resection of common bile duct and choledocho-jejunal anastomosis.
Subject(s)
Aged , Female , Humans , Bile Duct Neoplasms/diagnosis , Cholangiopancreatography, Magnetic Resonance , Mucins/metabolism , Papilloma/diagnosis , Tomography, X-Ray ComputedABSTRACT
Objective To evaluate the diagnostic and therapeutic effects of endoscopic retrograde cholangiopancreatography (ERCP) in biliary papillomatosis. Methods Data of 6 patients, who underwent ERCP and diagnosed as biliary papillomatosis from 2000 to 2008, were retrospectively analyzed. Results There were 3 males and 3 females, with the mean age of onset at 72.8 years (range 52-83 years). Recurrent cholangitis and jaundice were common presentations in all patients, with 5 patients having right upper abdominal pain and 3 others exhiting fever and algor. History of partial hepatectomy was observed in 2 patients. Endoscopic findings included dilated papillary orifice with mucin discharge in 5 patients and papillary-occupying lesion in 1 patient. Multiple filling defects in the lumen of the biliary system in dilated common bile duct were detected in all patients, accompanied with extra-hepatic ducts dilatation in 3, right intra-hepatic duct dilatation in 1, and major pancreatic duct dilation in 1. Of 6 patients, 5 underwent multiple ERCP, inclucling stents and endoscopic nasobiliary drainage (ENBD), and have survived for 10-30 months. Another 83-year-old patient underwent palliative endoscopic treatment with balloons, baskets and ENBD, but died of cholangitis 10 days after the procedure. Conclusion This case series reports the typical endoscopic findings of biliary papiliomatosis. For inoperable or postoperative recurrent patients, endoscopic palliative treatment is a safe, convenient and effective procedure.
ABSTRACT
No abstract available.
Subject(s)
Aged , Humans , Male , Bile Duct Neoplasms/diagnosis , Bile Ducts, Intrahepatic/pathology , Cholangiocarcinoma/diagnosis , Diagnosis, Differential , Mucins/metabolismABSTRACT
Biliary papillomatosis (BP) is an extremely rare condition that's characterized by multicenteric proliferations of adenomatous epithelium within the large bile ducts. Although BP is basically a collection of benign papillary adenoma, papillary adenocarcinoma can develop within these lesions, and it has a tendency to spread supericially along the bile duct mucosa. Such a malignancy is rare, but the prognosis is poor if it is impossible to completely remove the tumor. We report here on one case of multiple biliary papillomatosis in the biliary tree.
Subject(s)
Adenocarcinoma, Papillary , Adenoma , Bile Ducts , Biliary Tract , Epithelium , Mucous Membrane , Papilloma , PrognosisABSTRACT
No abstract available.
Subject(s)
Aged , Female , Humans , Bile Duct Neoplasms/diagnosis , Bile Ducts, Intrahepatic , Carcinoma, Papillary/diagnosis , Cholangiocarcinoma/diagnosisABSTRACT
Biliary papillomatosis (BP) is a rare disease that is classified as either the mucin-hypersecreting type or nonmucin-secreting type. Typical papillomas of the biliary tree mainly involve intrahepatic bile ducts or both intra- and extrahepatic bile ducts. The isolated involvement of the extrahepatic bile duct is rare, and there is no report of BP confined to the gallbladder in Korea. We report a case of a 50-year-old man who developed obstructive jaundice due to hypersecreted mucin from papillomas of the gallbladder.
Subject(s)
Humans , Middle Aged , Bile Ducts, Extrahepatic , Bile Ducts, Intrahepatic , Biliary Tract , Carcinoma, Papillary , Gallbladder , Jaundice, Obstructive , Korea , Mucins , Papilloma , Rare DiseasesABSTRACT
The mucin-hypersecreting bile duct tumor is rare and its clinical, radiologic, and pathologic features are not well known. We report the case of mucin-hypersecreting biliary papillomatosis with malignant transformation including review of 11 korean literatures. A 65-year-old female was admitted to our hospital with fever, chills, and right upper quadrant pain. A CT scan showed marked dilatation of left intrahepatic duct with intraductal filling defects. During endoscopic retrograde cholangiograpy, mucin from the ampulla was observed and dilated common bile duct with multiple amorphous filling defects was noted. Cholangioscopy revealed muliple coral-like mucosal papillary projections with large amount of mucin in the left intrahepatic ducts. The patient underwent left lobectomy, and the biopsy revealed intraductal papillary adenocarcinoma in the background of papillary adenoma.
Subject(s)
Aged , Female , Humans , Adenocarcinoma , Adenocarcinoma, Papillary , Adenoma , Bile Ducts , Biopsy , Chills , Common Bile Duct , Dilatation , Fever , Mucins , Papilloma , Tomography, X-Ray ComputedABSTRACT
Multiple biliary papillomatosis involves an epithelial field change of the intrahepatic and extrahepatic portions of the biliary tree. Pathologically it is benign, occasionally with dysplasia, but the clinical behavior is regarded as having a low-grade malignant potential. Such malignancy is rare but the prognosis is poor if it is impossible to remove the tumor completely. Here, we report one case of multiple biliary papillomatosis in the biliary tree.
Subject(s)
Biliary Tract , Papilloma , PrognosisABSTRACT
BACKGROUNDS AND STUDY AIMS: Multiple biliary papillomatosis (MBP) is an uncommon disease. This study was undertaken to review cases with respect to describing clinical features and characteristical cholangiographic findings, and to define the role of cholangioscopy in the diagnosis and treatment of this disorder. PATIENATS AND METHODS: from 1990 to 1997, nine patients (mean age; 57.3 years, 6 men and 3 women) were diagnosed as having MBP arnong 5,361 cases of endoscopic retrograde cholangiography (ERC) conducted at our center. A retrospective analyses of the cholangiographic and cholangioscopic findings as well as clinieal features were performed.