injury (trauma) of eye and orbit ( S05.-) Inflammation of the extraocular muscle of the eye. It is characterized by swelling which can lead to ischemia, fibrosis, or orbital pseudotumor. Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
Unspecified chronic inflammatory disorders of orbit. H05.10 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2020 edition of ICD-10-CM H05.10 became effective on October 1, 2019. This is the American ICD-10-CM version of H05.10 - other international versions of ICD-10 H05.10 may differ.
Presently, Nonspecific orbital inflammation and orbital inflammatory pseudotumor can be used interchangeably. NSOI is a benign noninfectious, inflammatory process of the orbit ; characterized by a polymorphous lymphoid infiltrate with varying degrees of fibrosis, without a known local or systemic cause. h
Orbital pseudotumor is the swelling of tissue behind the eye in an area called the orbit. The orbit is the hollow space in the skull where the eye sits. The orbit protects the eyeball and the muscles and tissue that surround it. Orbital pseudotumor does not spread to other tissues or places in the body.
2.
]. Orbital pseudotumor is an idiopathic condition of inflammation associated with many inflammatory and autoimmune conditions such as IgG4-related disease that can involve the extraocular muscles, lacrimal gland, other orbital structures and tissue.
After Graves' disease and lymphoproliferative disorders, orbital pseudotumor is the 3rd most common ophthalmologic disease of the orbit and account for approximately 8-11% of all the orbital tumors.
"Pseudotumor" means "false tumor." It's caused by increased pressure around the brain. It can be hard to tell a pseudotumor from a real tumor. So you should see your doctor to have your symptoms checked out. The symptoms of pseudotumor cerebri can get worse and hurt your vision.
ICD-10 code: G93. 2 Benign intracranial hypertension.
Orbital inflammatory disease (OID) represents a collection of inflammatory conditions affecting the orbit. OID is a diagnosis of exclusion, with the differential diagnosis including infection, systemic inflammatory conditions, and neoplasms, among other conditions.
Inflammatory pseudotumors (IPTs) are rare, well-circumscribed, unencapsulated, quasi-neoplastic tumors of unregulated growth of inflammatory cells, first recognized by Umiker and Iverson.
Differential Diagnosis 9 Thyroid eye disease is the most common cause of orbital inflammation in adults and has been found to account for nearly 60% of cases of orbital inflammation in the 21-60 year old age group. Orbital cellulitis risk factors include history of sinusitis, dental work/disease, or trauma.
Corticosteroids and surgical resection are the mainstays of therapy for inflammatory pseudotumors of the head and neck. High-dose corticosteroids cause rapid decrease of inflammatory pseudotumor, but tumors recurred in 20% of patients with parapharyngeal space or skull base treated with corticosteroids.
Idiopathic orbital inflammation (IOI) is a benign, non-infective clinical syndrome characterized by inflammation of the orbit without identifiable local or systemic disorders.[1] The exact etiology is unknown, but infection and immune mediated processes have been postulated.[1] Peak incidence of the disease is in ...
Non-specific orbital inflammation (NSOI) is defined as a benign inflammatory process of the orbit characterized by a polymorphous lymphoid infiltrate with varying degrees of fibrosis, without a known local or systemic cause.
Orbital myositis (OM) is an autoimmune disorder that is characterized by the inflammation of extraocular muscles. It presents with a limited clinical course and is considered to be a subtype of orbital inflammatory syndrome (1,2). This usually idiopathic disease is more common in middle-aged women.
Orbital apex syndrome (OAS) involves cranial neuropathies in association with optic nerve dysfunction. Orbital apex syndrome is symptomatically related to superior orbital fissure syndrome and cavernous sinus syndrome with similar etiologies. The distinction is the precise anatomic involvement of the disease process.
Orbital lymphoma refers to a lymphoma occurring in the conjunctiva, lacrimal gland, eyelid and ocular musculature. Primary non-Hodgkin's lymphoma (NHL) of the orbit is a rare presentation, representing 8-10% of extranodal NHL[1] and only 1% of all NHL. [2] Generally, it has an indolent course.
Ocular myositis describes a rare inflammatory disorder of single or multiple extraocular eye muscles. Primary manifestations encompass subacute orbital painful diplopia, exacerbated by eye movement. Diplopia is caused by handicapped contraction and distraction of affected eye muscles, not by neurogenic affection.
Nonspecific orbital inflammation was first described in 1905 by Birch-Hirschfeld. It was named as inflammatory pseudotumor in 1954 by Umiker et al. because of its propensity to mimic a malignant process. Presently, Nonspecific orbital inflammation and orbital inflammatory pseudotumor can be used interchangeably.
Nonspecific orbital inflammation (NSOI), also known as orbital inflammatory pseudotumor, idiopathic orbital inflammation ( IOI)and orbital inflammatory syndrome is the most common cause of painful orbital mass in adults. NSOI can be localized or diffuse.