A disorder marked by anemia caused by iron deficiency, and a web-like growth of membranes in the throat that makes swallowing difficult. Having plummer-vinson syndrome may increase the risk of developing esophageal cancer. A syndrome characterized by dysphagia, upper esophageal webs, iron deficiency anemia,...
When a type 2 excludes note appears under a code it is acceptable to use both the code (K22.8) and the excluded code together. esophageal varices ( ICD-10-CM Diagnosis Code I85 Paterson-Kelly syndrome ( ICD-10-CM Diagnosis Code D50.1
D50.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM D50.1 became effective on October 1, 2021.
2016 2017 2018 2019 Billable/Specific Code. K22.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2018/2019 edition of ICD-10-CM K22.8 became effective on October 1, 2018.
Plummer-Vinson syndrome is a condition that can occur in people with long-term (chronic) iron deficiency anemia. People with this condition have problems swallowing due to small, thin growths of tissue that partially block the upper food pipe (esophagus).
K22. 8 is a valid ICD-10-CM diagnosis code meaning 'Other specified diseases of esophagus'.
The diagnosis is based on the evidence of iron-deficiency anemia and one or more esophageal webs in a patient with postcricoid dysphagia. Esophageal webs can be detected by barium swallow X-ray but the best way for demonstration is the videofluoroscopy [11,37].
A disorder marked by anemia caused by iron deficiency, and a web-like growth of membranes in the throat that makes swallowing difficult. Having sideropenic dysphagia may increase the risk of developing esophageal cancer. Also called Paterson-Kelly syndrome and Plummer-Vinson syndrome.
ICD-10-CM Code for Gastro-esophageal reflux disease with esophagitis K21. 0.
Presbyesophagus is a term used to describe an abnormal shape of the swallowing tube (esophagus) that occurs in some individuals. In this situation, the esophagus appears wavier than a typically straight esophagus. This change may impact esophageal movement (motility).
A syndrome of DYSPHAGIA with IRON-DEFICIENCY ANEMIA that is due to congenital anomalies in the ESOPHAGUS (such as cervical esophageal webs).
Causes. The cause of Plummer–Vinson syndrome is unknown; however, genetic factors and nutritional deficiencies may play a role. It is more common in women, particularly in middle age, with a peak age over 50 years.
The Paterson-Brown-Kelly syndrome, also called the Plummer-Vinson syndrome or sideropenic dysphagia, consists of a triad of dysphagia, iron deficiency anemia, and esophageal webs. It was first described by Henry Stanley Plummer in the beginning of the 20th century and later on by Porter Paisley Vinson.
Atrophy of the gastric mucosa causes achlorhydria. atrophy of lingual papillae produces a smooth, shiny red tongue dorsum. There is a 10% incidence of splenomegaly associated with sideropenic anemia. The enlargement is minimal and pathogenesis is said to be unknown.
The syndrome is considered to be a precancerous condition because squamous cell carcinoma of hypopharynx, upper esophagus, or oral cavity takes place in 10% of these patients.
Introduction. Post cricoid web is rare in males when compared to females. Females present with oesophageal web as part of Plummer Vinson syndrome. The web causes dysphagia, initially intermittent, but later constant with no other symptoms.