| Pancreatic disease |
| Classification and external resources |
| Specialty |
gastroenterology |
| ICD-10 |
K85-K86, Q45.0-Q45.3 |
| ICD-9-CM |
577, 751.7 |
| MeSH |
D010182 |
|
[edit on Wikidata]
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Pancreatic diseases include:
Contents
- 1 Pancreatitis
- 2 Diabetes mellitus
- 3 Exocrine pancreatic insufficiency
- 4 Cystic fibrosis
- 5 Pseudocysts
- 6 Cysts
- 7 Congenital malformations
- 7.1 Pancreas divisum
- 7.2 Annular pancreas
- 8 Neoplasms
- 8.1 Benign
- 8.2 Tumor predisposition
- 8.2.1 Zollinger-Ellison syndrome
- 9 Hemosuccus pancreaticus
- 10 See also
- 11 References
Pancreatitis
Pancreatitis is inflammation of the pancreas. There are two forms of pancreatitis, which are different in causes and symptoms, and require different treatment:
- Acute pancreatitis is a rapid-onset inflammation of the pancreas, most frequently caused by alcoholism or gallstones.
- Chronic pancreatitis is a long-standing inflammation of the pancreas.
Diabetes mellitus
The pancreas is central in the pathophysiology of both major types of diabetes mellitus. In type 1 diabetes mellitus, there is direct damage to the endocrine pancreas that results in insufficient insulin synthesis and secretion. Type 2 diabetes mellitus, which begins with insulin resistance, is characterized by the ultimate failure of pancreatic β cells to match insulin production with insulin demand.
Exocrine pancreatic insufficiency
Exocrine pancreatic insufficiency (EPI) is the inability to properly digest food due to a lack of digestive enzymes made by the pancreas. EPI is found in humans afflicted with cystic fibrosis and Shwachman–Diamond syndrome. It is caused by a progressive loss of the pancreatic cells that make digestive enzymes. Chronic pancreatitis is the most common cause of EPI in humans. Loss of digestive enzymes leads to maldigestion and malabsorption of nutrients.
Cystic fibrosis
Cystic fibrosis, is a hereditary disease that affects the entire body, causing progressive disability and early death. It is caused by a mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The product of this gene helps create sweat, digestive juices, and mucus. The name cystic fibrosis refers to the characteristic 'fibrosis' (tissue scarring) and cyst formation within the pancreas, causing irreversible damage, and often resulting in painful inflammation (pancreatitis).
Pseudocysts
A pancreatic pseudocyst is a circumscribed collection of fluid rich in amylase and other pancreatic enzymes, blood and necrotic tissue, typically located in the lesser sac.
Cysts
X-ray computed tomography (CT scan) findings of cysts in the pancreas are common, and often are benign. In a study of 2,832 patients without pancreatic disease, 73 patients (2.6%) had cysts in the pancreas.[1] About 85% of these patients had a single cyst. Cysts ranged in size from 2 to 38 mm (mean, 8.9 mm). There was a strong correlation between the presence of cysts and age. No cysts were identified among patients less than 40 years of age, while 8.7 percent of the patients aged 80 to 89 years had a pancreatic cyst.
Cysts also may be present due to intraductal papillary mucinous neoplasm.
Congenital malformations
Pancreas divisum
Pancreas divisum is a malformation in which the pancreas fails to fuse. It is a rare condition that affects only 6% of the world's population, and of these few, only 1% ever have symptoms that require surgery.
Annular pancreas
Annular pancreas is characterized by a pancreas that encircles the duodenum. It results from an embryological malformation in which the early pancreatic buds undergo inappropriate rotation and fusion, which can lead to small bowel obstruction.
Neoplasms
See pancreatic tumors, benign or malignant (pancreatic cancer).
Benign
- Serous cystadenoma of the pancreas
- Solid pseudopapillary neoplasm
Tumor predisposition
Zollinger-Ellison syndrome
Zollinger-Ellison syndrome is a collection of findings in individuals with gastrinoma, a tumor of the gastrin-producing cells of the pancreas. Unbridled gastrin secretion results in elevated levels of the hormone, and increased hydrochloric acid secretion from parietal cells of the stomach. It can lead to ulceration and scarring of the stomach and intestinal mucosa.
Hemosuccus pancreaticus
Hemosuccus pancreaticus, also known as pseudohematobilia or Wirsungorrhage, is a rare cause of hemorrhage in the gastrointestinal tract. It is caused by a bleeding source in the pancreas, pancreatic duct, or structures adjacent to the pancreas, such as the splenic artery, that bleed into the pancreatic duct. Patients with hemosuccus may develop symptoms of gastrointestinal hemorrhage, such as blood in the stools, maroon stools, or melena. They may also develop abdominal pain. Hemosuccus pancreaticus is associated with pancreatitis, pancreatic cancer and aneurysms of the splenic artery. Angiography may be used to diagnose hemosuccus pancreaticus, where the celiac axis is injected to determine the blood vessel that is bleeding. Concomitant embolization of the end vessel may terminate the hemorrhage. Alternatively, a distal pancreatectomy may be required to stop the hemorrhage.
See also
References
- ^ Laffan T, Horton KM, Klein AP, et al. (Sep 2008). "Prevalence of unsuspected pancreatic cysts on MDCT". AJR Am J roentgenol. 191 (3): 802–807. PMC 2692243 . PMID 18716113. doi:10.2214/AJR.07.3340.
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Congenital malformations and deformations of digestive system (Q35–Q45, 749–751)
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| Upper GI tract |
| Tongue, mouth and pharynx |
- Cleft lip and palate
- Van der Woude syndrome
- tongue
- Ankyloglossia
- Macroglossia
- Hypoglossia
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| Esophagus |
- EA/TEF
- Esophageal atresia: types A, B, C, and D
- Tracheoesophageal fistula: types B, C, D and E
- esophageal rings
- Esophageal web (upper)
- Schatzki ring (lower)
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| Stomach |
- Pyloric stenosis
- Hiatus hernia
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| Lower GI tract |
| Intestines |
- Intestinal atresia
- Meckel's diverticulum
- Hirschsprung's disease
- Intestinal malrotation
- Dolichocolon
- Enteric duplication cyst
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| Rectum/anal canal |
- Imperforate anus
- Rectovestibular fistula
- Persistent cloaca
- Rectal atresia
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| Accessory |
| Pancreas |
- Annular pancreas
- Accessory pancreas
- Johanson–Blizzard syndrome
- Pancreas divisum
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| Bile duct |
- Choledochal cysts
- Biliary atresia
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| Liver |
- Alagille syndrome
- Polycystic liver disease
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