icd 10 code for henoch schonlein purpura

What is Henoch-Schönlein purpura?

ICD-10-CM Diagnosis Code D69.0 [convert to ICD-9-CM] Allergic purpura. Glomerulonephritis due to henoch schonlein purpura; Henoch-schˆnlein purpura; Henoch-schönlein purpura; Purpura, henoch schonlein; thrombocytopenic hemorrhagic purpura (D69.3); Allergic vasculitis; Nonthrombocytopenic hemorrhagic purpura; Nonthrombocytopenic idiopathic purpura; …

What is the ICD-10 code for Henoch-Schönlein disease?

Dec 29, 2019 · T80 Complications following infusion, henoch schonlein purpura icd 10 code for hypothyroidism A Non-ABO incompatibility reaction due to trans Benign primary hypergammaglobulinemic purpura ; Hypergammaglobulinemia, polyclonal; Purpurahypergammaglobulinemic, benign primary; Benign hypergammaglobulinemic purpura ; …

What is the ICD 10 code for purpura?

The ICD code D690 is used to code Henoch-Schönlein purpura. Henoch–Schönlein purpura (HSP, also known as anaphylactoid purpura, purpura rheumatica, and Schönlein–Henoch purpura) is a disease of the skin and other organs that most commonly affects children. In the skin, the disease causes palpable purpura (small hemorrhages); often with joint and abdominal pain.

What is allergic purpura?

Jun 18, 2015 · ICD-10 Code: D69.0. Definition: Henoch-Schönlein purpura is a systemic, small-vessel vasculopathy affecting the skin (lower extremities), gut, and kidneys. Henoch-Schönlein purpura is classically characterized by the triad of nonthrombocytopenic purpura, arthralgia, and abdominal pain. Etiology: The cause of Henoch-Schönlein purpura is unknown; it is labeled as …

What is the ICD-10 code for HSP?

ICD-10-CM Code for Allergic purpura D69. 0.

What is the ICD-10 code for Purpura?

D69. 0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is the ICD-10 code for Leukocytoclastic vasculitis?

Vasculitis (Leukocytoclastic Vasculitis) (08) leg [ICD-10 L95. 9] Leukocytoclastic vasculitis, also known as hypersensitivity vasculitis, is an inflammation of blood vessels that forms small lesions on the skin. The direct cause is unknown, but vasculitis is often linked to autoimmune disorders.

What is the correct ICD-10 code for thrombocytopenia?

ICD-10 | Thrombocytopenia, unspecified (D69. 6)

What is solar purpura?

Solar purpura (say "PURR-pyuh-ruh" or "PURR-puh-ruh") is a condition that causes one or more flat, purple bruises. It often occurs on the hands, forearms, and legs. Purpura is common in older people. It is called solar purpura because it occurs most often on areas that are exposed to the sun.

What is meant by senile purpura?

Senile purpura is a common, benign condition characterised by the recurrent formation of purple ecchymoses (bruises) on the extensor surfaces of forearms following minor trauma.

What is lymphocytic vasculitis?

Lymphocytic vasculitis is one of several skin conditions which are collectively referred to as cutaneous vasculitis. In lymphocytic vasculitis, white blood cells ( lymphocytes ) cause damage to blood vessels in the skin.

What is the ICD 10 for UTI?

Urinary tract infection, site not specified N39. 0 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 N39. 0 became effective on October 1, 2021.

What is necrotizing vasculitis?

Necrotizing vasculitis is a group of disorders that involve inflammation of the blood vessel walls. The size of the affected blood vessels helps to determine the names of these conditions and how the disorder causes disease.May 2, 2021

What is the ICD-10 code for esophageal varices?

Esophageal varices with bleeding I85. 01 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is the difference between primary and secondary thrombocytopenia?

ITP is an autoimmune bleeding disorder caused by various etiologies, which is characterized by increased platelet destruction and impaired production, resulting in a decreased platelet count. Primary ITP is idiopathic, whereas secondary ITP is linked to an underlying condition (1).Jun 24, 2021

What is the ICD-10 code for acute on chronic thrombocytopenia?

ICD-10-CM Code for Thrombocytopenia, unspecified D69. 6.

What is the Henoch-Schonlein purpura registry?

The Autoimmune Registry supports research for Henoch-Schonlein purpura by collecting information about patients with this and other autoimmune diseases. You can join the registry to share your information with researchers and receive updates about participating in new research studies. Learn more about registries.

What causes Henoch-Schonlein purpura?

The cause of Henoch-Schonlein purpura (HSP) is not completely understood, but research indicates that genes play a key role in predisposing a person to developing HSP, as well as the severity of HSP in each person. [1] The disease has been most strongly associated with having certain variations of genes in the human leukocyte antigen (HLA) gene family, a cluster of genes that the immune system uses to tell the difference between the body's own substances and foreign invaders. [1] Environmental factors such as recent bacterial or viral infections, food allergies, and medication reactions also may play a role in the onset of HSP in people who are genetically predisposed. [1] [4]

What is HSP in medical terms?

Henoch-Schonlein purpura (HSP), also called immunoglobulin A vasculitis (IgAV), is a vascular disease that primarily affects small blood vessels. The disease is characterized by abnormal deposits of immunoglobulin A (an antibody) in the blood vessels, leading to their inflammation (vasculitis). The small vessels of the skin, joints, kidneys, ...

How long does it take to recover from HSP?

The vast majority of people with Henoch-Schonlein purpura (HSP) recover on their own within several weeks. [2] [5] [8] Supportive care until recovery when there is little or no kidney involvement may include adequate hydration, rest, and over-the-counter pain medication as needed for joint and abdominal pain due to inflammation. Swelling of the lower body may improve with bed rest or elevating the affected area of the body. If symptoms of inflammation are severe, prescription pain or anti-inflammatory medication may be needed. [8] Non-steroidal anti-inflammatory drugs (NSAIDs) should not be used in people with impaired kidney function or kidney disease. [9] Rarely, severe gastrointestinal complications require surgery. [3]

What is the HPO database?

People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources.

Is HSP inherited?

However, while genes may increase the risk of developing the disease (and in some cases more than one family member has HSP), the disease itself is not inherited. [1] [3] Environmental “triggers” such as foods, infections, or medications may also play a role in the onset of the disease. [1] [4] [5] The diagnosis of HSP may be made based on ...

What is the HLA gene?

The disease has been most strongly associated with having certain variations of genes in the human leukocyte antigen (HLA) gene family, a cluster of genes that the immune system uses to tell the difference between the body's own substances and foreign invaders. [1] .