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Foster Kennedy syndrome anosmia

Foster Kennedy Syndrome - an overview ScienceDirect Topic

The patient had right-sided anosmia. magnetic resonance imaging showed a lesion in the frontal lobe that was deviated to the right and attached to the olfactory groove. A histopathologic study of the excised specimen disclosed a meningioma. We believe that this patient wit Foster Kennedy was the first to correlate the signs of unilateral optic atrophy and contralateral papilledema to basofrontal expanding lesions and stress its value in localizing the lesions Foster-Kennedy Syndrome is characterized by the compression of the ipsilateral optic nerve by an intracranial mass, often an anterior cranial fossa meningioma (e.g., frontal lobe, olfactory groove, sphenoid wing). When the intracranial mass is large enough however to elevate intracranial pressure, contralateral papilledema results Well then smashedpea's blog reminded me, Foster Kennedy Syndrome. It refers to a constellation of findings associated with tumors of the frontal lobe. Apparently it is quite exciting for neuro medical types. I had no symptoms of it before, but I do now, aka, no sense of smell Anosmia. Posted by Sarah Ramsden Esthesioneuroblastoma is an exceedingly rare cancerous tumor that originates in or near the olfactory nerve. Symptoms are anosmia (loss of sense of smell) often accompanied by chronic sinusitis. Intranasal drug use; Samter's triad also known as AERD (aspirin exacerbated respiratory disease) Foster Kennedy syndrome; Cadmium poisoning; Smokin

Foster Kennedy Syndrome Due to Meningioma Growth during

Clinical and computed tomographic findings in the Foster

Foster Kennedy syndrome is a very rare syndrome which includes ipsilateral optic atrophy and central scotoma, anosmia, contralateral papilledema, and, occasionally, ipsilateral proptosis. [ncbi.nlm.nih.gov] Ken·ne·dy syn·drome ( ken'ĕ-dē ), ipsilateral optic atrophy with central scotoma and contralateral choked disc or papilledema, caused by a meningioma of the ipsilateral optic nerve Anosmia can be due to a number of factors, including an inflammation of the nasal mucosa, blockage of nasal passages or a destruction of one temporal lobe. Inflammation is due to chronic mucosa changes in the lining of the paranasal sinus and in the middle and superior turbinates

Foster Kennedy Syndrome: Now and Then. Diffusion Tensor Imaging in Traumatic Optic Tract Syndrome. Restricted Diffusion in Isolated Superior Ophthalmic Vein Thrombosis. The Immunopathology of Giant Cell Arteritis: Diagnostic and Therapeutic Implications Loss of smell without a cold is one of the clinical symptoms: the syndrome of Pehkrantz (adiposogenital dystrophy, which develops due to the defeat of the hypothalamus); Foster-Kennedy Syndrome; epilepsy, a significant increase in intracranial pressure, dementia (including Lewy bodies), Alzheimer's disease Kallmann syndrome (KS) is a rare genetic disorder characterized by hypogonadotropic hypogonadism associated with anosmia or hyposmia. When anosmia is absent it is simply referred to as idiopathic hypogonadotropic hypogonadism (IHH). Foster Kennedy syndrome describes the clinical syndrome of unilateral optic atrophy with contralateral. Anosmia, or the loss of the sense of smell, is common and affects most people at some point in life. Hormone related: Thyroid gland dysfunction, Kallmann syndrome. (Foster Kennedy Syndrome). Neurological problems: Alzheimer's and Parkinson diseases. Age related loss (presbyosmia). Is Anosmia a serious condition Foster kennedy syndrome Seen in olfactory groove or sphenoidal ridge meningiomas or frontal lobe ICSOL 3 signs-Ipsilateral anosmia -Ipsilateral optic atrophy -Contralateral papilledema 28

Foster Kennedy Syndrome: Now and Then : Journal of Neuro

  1. • Mass lesions around the olfactory region can result in a Foster-Kennedy syndrome, which consists of: (1) ipsilateral anosmia; (2) ipsilateral optic atrophy and (3) contralateral papilloedema (d/t raised intracranial pressure.) 17
  2. Foster-Kennedy syndrome. Etiology. Frontal lobe tumors, typically parasellar or subfrontal meningiomas; Olfactory groove meningioma; : meningiomas arising from the cribriform plate and frontosphenoidal suture (see meningiomas) Clinical features. Ipsilateral atrophy of the optic nerve; Contralateral papilledema; Anosmia; Orbital apex syndrome
  3. Compressive Optic Disc Edema and Contralateral Papilledema: Type 2 Foster Kennedy Variant Syndrome. J Neuroophthalmol. 2021 Jun 1;41 (2):e217-e219. doi: 10.1097/WNO.0000000000001091
  4. association with anosmia. It has been described by numerous of authors such as: William Gower in 1893, Schultz-Zehden in 1905, Foster Kennedy in 1911 in USA then later the depiction done by Willehm Uhthoff in 1915.Regarding the importance of this syndrome caused by cerebral tumor, we relate 2 clinical cases found durin
  5. Foster Kennedy syndrome (FKS) is a very rare neurological syndrome with a unique ophthalmological manifestation described in 1911 by Robert Foster Kennedy attributed to Anosmia results from direct compression of the olfactory nerve. (1, 2) We describe a case report regarding th

contralateral papilledema and anosmia was first fully described by Kennedy in 1911, also known as Gower-Paton-Kennedy syndrome [3]. Anosmia is often included in the syndrome but its presence has not been universally reported as in our patient. Foster Kennedy syndrome is known to be caused by multiple intracranial pathologies Foster Kennedy syndrome, named after neurologist Robert Foster Kennedy (1884-1952), describes unilateral ipsilat-eral optic atrophy and contralateral papilledema from an intracranial mass. This syndrome is unreliably associated with anosmia and ipsilateral proptosis [1]. It originates from variety of intracranial pathologies, but most often The Foster Kennedy syndrome then became a triad consisting of ipsilateral optic atrophy, contralateral disc edema, and ipsilateral anosmia. This syndrome is due to optic nerve compression, olfactory nerve compression, and increased intracranial pressure (ICP) secondary to a space occupying lesion (such as meningioma or plasmacytoma, usually an. The patient may present with anosmia and frontal lobe signs alongside the visual symptoms (central scotoma). In the absence of intracranial mass, the above mentioned findings are named pseudo- Foster Kennedy Syndrome. It is classically due to bilateral sequential optic neuritis/ischemic optic neuropath

Foster Kennedy syndrome - Wikipedi

  1. The original 1911 description of the Foster Kennedy syndrome included the triad of optic disc pallor in one eye, optic disc edema in the fellow eye, and anosmia or hyposmia in association with anterior cranial fossa mass lesions ().The pathogenesis of the optic disc pallor was believed to be direct compression of the prechiasmatic optic nerve
  2. True Foster Kennedy syndrome is the combination of papilledema in one eye and pallor in the other eye due to a large mass lesion causing compressive optic neuropathy and increasing intracranial pressure. True Foster Kennedy syndrome is very rare, and is typically caused by an olfactory groove meningioma
  3. B12 plays an important role in DNA synthesis, and its deficiency causes peripheral neuropathy, myeloneuropathy, and, very rarely, optic neuropathy
  4. Foster Kennedy syndrome secondary to oligodendroglioma - Grand Rounds Foster Kennedy syndrome secondary to oligodendroglioma - Foster Kennedy syndrome (FKS) is rare. It is characterised by the presence of ipsilateral optic atrophy, contralateral papilloedema and ipsilateral anosmia. Since its first description in 1911, it has never been reported in oligodendroglioma

Foster Kennedy syndrome and optociliary shunt vessels in a

  1. Pseudo-Foster-Kennedy syndrome is defined as one sided optic atrophy with papilledema in the other eye but with the absence of intracranial mass lesion. Case report A 67 year old male presented to our OPD with complaints of dimness of vision in right eye since 12 weeks and dimness of vision in left eye since 3 weeks
  2. B12 plays an important role in DNA synthesis, and its deficiency causes peripheral neuropathy, myeloneuropathy, and, very rarely, optic neuropathy
  3. Anosmia and headache are often present in true Foster Kennedy syndrome ; however, they are not universally present signs. Other common complications depend on the area of intracranial involvement and potentially include emotional lability, memory loss, nausea, vomiting, vertigo, hearing loss, extremity weakness, and facial paresis
  4. Robert Foster Kennedy Sir William Richard Gowers Condition characterised by unilateral ipsilateral atrophy with contralateral papilloedema, central scotoma, and anosmia (absence of the sense of smell) usually due to a frontal lobe tumour or a meningioma of the optic nerve
  5. ded me, Foster Kennedy Syndrome. It refers to a constellation of findings associated with tumors of the frontal lobe. Apparently it is quite exciting for neuro medical types. I had no symptoms of it before, but I do now, aka, no sense of smell Anosmia

Foster Kennedy syndrome: A case report with literature

Pseudo-Foster Kennedy Syndrome is defined as unilateral optic atrophy with optic disc swelling in the contralateral eye in the ab-sence of an intracranial mass. We reported an uncommon manifes-tation of nonarteritic ischemic optic neuropathy presenting as Pseu-do-Foster Kennedy Syndrome in a fifty years old male A 48-year-old woman complained of acute loss of vision in her right eye. Ophthalmoscopically, the right optic disk appeared pale, and abnormally dilated vessels were noted on the disk. The left optic disk was reddish and swollen. Fluorescein angiography revealed abnormal vessels on the right optic disk that might be venous. The patient had right-sided anosmia. Computed tomography and magnetic. Testing the hearing in a patient with retinitis pigmentosa in Usher's syndrome. Testing the sense of smell in a patient with optic atrophy in one eye and papilloedema in the other. (This is because sphenoidal ridge meningioma can give rise to Foster-Kennedy's Syndrome and anosmia)

Foster-Kennedy vs Pseudo-Foster-Kennedy - EyeWik

  1. disparity. Anosmia results from concomitant compression of the proximal olfactory nerve. The fun-doscopic findings, although rare, have been reported in various tumors and nontumor condi-tions,1-7 and pseudo-Foster Kennedy syndrome or Foster Kennedy sign has been suggested as a more accurate designation of the isolated ocular manifestation
  2. B12 plays an important role in DNA synthesis, and its defi-ciency causes peripheral neuropathy, myeloneuropathy, and, very rarely, optic neuropathy
  3. 32. Compression is seen in Foster Kennedy syndrome 32-A. Foster Kennedy syndrome involves the olfactory tract and the optic nerve. This disorder may be due to a tumor (olfactory groove meningioma). The signs are ipsilateral anosmia, ipsilateral optic atrophy, and contralateral papilledema. 1. A 40-year old woman presents with brief severe headaches over the right eye
  4. Foster-Kennedy syndrome. Foster-Kennedy syndrome (also known as Gowers-Paton-Kennedy syndrome, Kennedy's phenomenon or Kennedy's syndrome) refers to a constellation of findings associated with tumors of the frontal lobe. New!!: Anosmia and Foster-Kennedy syndrome · See more » Frontal lob
  5. Foster Kennedy syndrome is a constellation of findings associated with tumors of the frontal lobe. Although Foster Kennedy syndrome is sometimes called Kennedy syndrome, it should not be confused with Kennedy disease, or anosmia (loss of smell) ipsilaterally
Pseudo-Foster Kennedy Syndrome: A Rare Presentation of

Foster Kennedy syndrome is a constellation of findings associated with tumors of the frontal lobe.. Although Foster Kennedy syndrome is sometimes called Kennedy syndrome, it should not be confused with Kennedy disease, or spinal and bulbar muscular atrophy, which is named after William R. Kennedy. Pseudo-Foster Kennedy syndrome is defined as one-sided optic atrophy with papilledema in the. THE FOSTER KENNEDY SYNDROME AN EVALUATION OF ITS DIAGNOSTIC VALUE FRITZ VON \\VOWERN A symptom complex of unilateral optic atrophy with central scotoma and contralateral papilloedema was described by Schultz-Sehden in 1905, and Gowers (1909) and Paton (1909) observed the same symptoms in one and three patients respectively. Foster Kennedy (1911) was the first to consider the combination as a.

Foster Kennedy's syndrome is a constellation of symptoms and signs associated with tumors of the frontal lobe of the brain. Anosmia (loss of smell) The symptoms of intracranial pressure include Foster-kennedy-syndrome Symptom Checker: Possible causes include Meningioma. Check the full list of possible causes and conditions now! Talk to our Chatbot to narrow down your search

Anosmia can be associated with other medical conditions such as nasal polyps, tumors, allergies, Parkinson's disease, Alzheimer's disease, Foster Kennedy syndrome etc. Even zinc deficiency can induce anosmia. And finally, irritants and toxins (e.g. cadmium poisoning) as well as abuse of nasal decongestants may cause anosmia in previously. Intracranial meningiomatosis causing foster kennedy syndrome by unilateral optic nerve compression and blockage of the superior sagittal sinus. Increased anti-saccade latency is an isolated lingering abnormality in Sydenham chorea Foster Kennedy syndrome is a very rare syndrome which includes ipsilateral optic atrophy and central scotoma, anosmia, contralateral papilledema, and, occasionally, ipsilateral [ncbi.nlm.nih.gov] [] meningioma 26 8 Reply optic atrophy and anosmia due to compression of optic and olfactory nerves, respectivaly Foster Kennedy syndrome refers to a constellation of findings associated with brain tumors involving the frontal lobe. Historical Perspective. The syndrome was first extensively noted by Robert Foster Kennedy in 1911, a British neurologist, anosmia (loss of smell) ipsilaterally

A: Foster-Kennedy syndrome refers to a syndrome that pressure from a frontal lobe tumor or olfactory meningioma causes optic atrophy on the side of the tumor, along with a papilloedema on the other side owing to the raised intracranial pressure. The syndrome is generally incomplete, and this ipsilateral optic atrophy is classically associated. Anosmia (pronounced / æ n ˈ ɒ z m i ə /) is [[an olfaction disorder and is the inability to perceive odor, or in other words a lack of functioning olfaction.Anosmia may be temporary but traumatic anosmia can be permanent. Anosmia is due to an inflammation of the nasal mucosa; blockage of nasal passages or a destruction of one temporal lobe.Specifically, according to The Lancet journal. Foster Kennedy Syndrome is a constellation of signs that classically includes unilateral compressive optic atrophy, contralateral papilledema, anosmia, and the presence of an intracranial lesion. The syndrome is most frequently from meningiomas but may also be due to gliomas, frontal lobe abscesses, plasmacytomas, nasopharyngeal angiofibromas. About Press Copyright Contact us Creators Advertise Developers Terms Privacy Policy & Safety How YouTube works Test new features Press Copyright Contact us Creators.

Intern Emerg Med (2011) 6:267-269 DOI 10.1007/s11739-010-0437-y CE - M EDI C AL ILLUSTRATION An unusual presentation of subfrontal meningioma: a case report and literature review for Foster Kennedy syndrome • • • Shahram Lotfipour Kris Chiles J. Akiva Kahn Tareg Bey Scott Rudkin Received: 17 December 2009 / Accepted: 13 July 2010 / Published online: 26 August 2010 SIMI 2010. Foster Kennedy syndrome is a constellation of findings associated with tumors of the frontal lobe. [1] Although Foster Kennedy syndrome is sometimes called 'Kennedy syndrome', [2] it should not be confused with Kennedy disease, or spinal and bulbar muscular atrophy, which is named after William R. Kennedy. Pseudo-Foster Kennedy syndrome is defined as one-sided optic atrophy with papilledema in. A Síndrome de Foster Kennedy compreende uma gama de sintomas originados por um tumor presente na fossa anterior do cérebro que gera compressão dos nervos olfatório e óptico. Os sinais clássicos da síndrome compreendem atrofia de disco óptico ipsilateral associada a papiledema contralateral. [1] Outros sinais e sintomas incluem cefaleia, hiposmia ou anosmia, náuseas, vômitos e. Foster Kennedy syndrome - medicine.en-academic.com Kennedy

Foster Kennedy syndrome is a constellation of findings associated with tumors of the frontal lobe. [1] Although Foster Kennedy syndrome is sometimes called 'Kennedy syndrome', [2] it should not be confused with Kennedy disease, or spinal and bulbar muscular atrophy, which is named after William R. Kennedy A 52-year-old man had progressive loss of visual acuity in his left eye associated with anosmia of five years duration. Clinical findings included papilledema in the right eye and optic atrophy in the left eye. A diagnosis of Foster Kennedy syndrome was made. Careful attention to the ophthalmoscopic. Foster-Kennedy syndrome (also known as Gowers-Paton-Kennedy syndrome, Kennedy's phenomenon or Kennedy's syndrome) refers to a constellation of findings associated with tumors of the frontal lobe.. Although Foster-Kennedy syndrome is equated with Kennedy syndrome, it should not be confused with Kennedy disease, which is named for William R. Kennedy Foster Kennedyn oireyhtymä on etulohkon kasvaimiin liittyvä havainto. Vaikka Foster Kennedyn oireyhtymää kutsutaan joskus Kennedyn oireyhtymäksi, sitä ei pidä sekoittaa Kennedy-tautiin tai selkärangan ja sipulien lihasten surkastumiseen , joka on nimetty William R.Kennedyn mukaan. Pseudo-Foster Kennedyn oireyhtymä määritellään yksipuoliseksi optiseksi atrofiaksi , jossa. Foster-Kennedy Syndrome (FKS) is a relatively rare clinical entity, first described by Kennedy F. et al (5). FKS is defined by presences of ipsilateral optic atrophy and contralateral papilledema, and occasionally anosmia. FKS is said to be due to an intracranial lesion causin

Foster Kennedy Syndrome Me, Myself, & Meningiom

Foster Kennedy syndrome I and II Optic atrophy, central scotoma in the ipsilateral eye, papilledema in the controlateral eye, anosmia Medial skull base Sphenoidale syndrome: III, IV, V 1 and VI Because of the close proximity of the anatomical structures, these syndromes frequentl Kennedy's disease is an inherited motor neuron disease that affects males. It is one of a group of disorders called lower motor neuron disorders (which involve disruptions in the transmission of nerve cell signals in the brain to nerve cells in the brain stem and spinal cord). Onset of the disease is usually between the ages of 20 and 40.

Foster Kennedy syndrome in a 52-year-old woman. (A) Fundus picture of the right eye showing optic disc pallor.(B) Fundus picture of the left eye showing disc oedema with tortuosity of the peripapillary vessels.(C and D) T2 weighted MRI images in axial and sagittal view demonstrating a extra-axial, well circumscribed, homogenous, isointense mass lesion in the fronto-parietal cortex with broad. Search Google Scholar; Export Citation; 6. Kennedy, F. A further note on the diagnostic value of retrobulbar neuritis in expanding lesions of the frontal lobes, with a report of this syndrome in a case of aneurysm of the right internal carotid artery Kennedy disease is a rare, X-linked slowly progressive neuromuscular disorder. Kennedy disease is typically an adult-onset disease, where symptoms occur mainly between the ages of 20 and 50. The disease is characterized by symptoms such as muscle weakness and cramps in the arms, legs, and facial area, enlarged breasts, and difficulty with.

What results from Foster Kennedy Syndrome? Ipsilateral anosmia, optic atrophy, and contralateral papilledema What must the chemical substances be dissolved in to excite the receptors for smell and taste Since the pandemic was declared in early 2020, COVID-19-related anosmia quickly emerged as a telltale sign of infection. 1,2 However, the time course and reversibility of COVID-19-related olfactory disorders, which may persist and negatively affect patients' lives, require further study. To clarify the clinical course and prognosis, we followed a cohort of patients with COVID-19. True Foster Kennedy syndrome is rare, but other causes of unilateral disc edema with contralateral optic pallor are more common. These have been termed pseudo-Foster Kennedy syndrome, or PFK. This review will present a recent case report of PFK and discuss differential diagnosis and management of the condition. Case Repor La Foster-Kennedy è una sindrome orbito-frontale e può esordire con uno dei sintomi tipici di questa categoria sindromica. Le caratteristiche peculiari sono invece l' anosmia unilaterale provocata da compressione sulla corteccia entorinale o sui bulbi olfattivi , atrofia ottica unilaterale per compressione del nervo ottico e papilla da stasi. Download PDF. Foster Kennedy syndrome was first described in 1911 by the neurologist Robert Foster Kennedy, who characterized the disorder as compression of one optic nerve by a subfrontal meningioma, resulting in optic nerve head pallor, with increased intracranial pressure causing contralateral optic nerve head edema. 1 True Foster Kennedy syndrome is rare, but other causes of unilateral.

A Unique Case of Sinonasal Teratocarcinosarcoma Presenting as Foster Kennedy Syndrome - Volume 46 Issue 3. Skip to main content Accessibility help We use cookies to distinguish you from other users and to provide you with a better experience on our websites Pseudo-Foster Kennedy syndrome is defined as ipsilateral optic atrophy with disc edema in the contralateral eye with absence of intracranial mass [1]. It has been usually reported in cases of Benign Intracranial hypertension [2]. Ischemic optic neuropathies and Optic nerve hypoplasia in literature Prior to a discussion of the syndrome, we review the life of Robert Foster Kennedy, MD. PERSONAL HISTORY Robert Foster Kennedy (Figure) was born in Belfast, Ireland, on Feb 7, 1884. His grandfather was a professor at the Royal University of Ireland, Belfast Foster-Kennedy syndrome refers to a syndrome that pressure from a frontal lobe tumor or olfactory meningioma causes optic atrophy on the side of the tumor, along with a papilloedema on the other side owing to the raised intracranial pressure.The syndrome is generally incomplete, and this ipsilateral optic atrophy is classically associated with a central scotoma and anosmia Bhatnagar KP, Kennedy RC, Baron G, Greenberg RA. Number of mitral cells and the bulb volume in the aging human olfactory bulb: a quantitative morphological study. Anat Rec . 1987 May. 218(1):73-87

Foster Kennedy syndrome 61, 134 Friedreich's ataxia 186 frontal lobe epilepsy 138 fMRI 97 function in olfaction 23 injury 219 MRI scan 3 shear force 124-5 trauma 125, 127 see also orbitofrontal cortex fungal infection 123, 226-7 furfural, anosmia 38 GABA 20 gabapentin 218 gadolinium-DTPA 91 galaxolide, demographic differences in perception 4 The syndrome was first described in 1911 by the neurologist. Foster Kennedy, who presented a series of six patients with the triad of ipsilateral optic atrophy, contralateral papilloedema and ipsilateral anosmia [3] . It is usually caused by a large, frontal lobe

Anosmia ~ Nursing Brai

Anosmia: | | | Anosmia | | | | Classificatio... World Heritage Encyclopedia, the aggregation of the largest online encyclopedias available, and the most definitive. Anosmia Classification and external resources Specialty: Neurology: ICD-10: R43.0 ICD-9-CM: 781.1 MeSH: D000857 Anosmia is the inability to perceive odor or a lack of functioning olfaction.

Frontiers Foster Kennedy Syndrome Due to Meningioma

View Academics in Foster Kennedy Syndrome on Academia.edu Anosmia is the inability to perceive odor or a lack of functioning olfaction—the loss of the sense of smell. Anosmia may be temporary, but some forms such as those from an accident can be permanent. Anosmia is due to a number of factors, including an inflammation of the nasal mucosa, blockage of nasal passages or a destruction of one temporal lobe. Inflammation is due to chronic mucosa. Journal Français d'Ophtalmologie - Vol. 42 - N° 9 - p. 1020-1021 - Foster-Kennedy Syndrome - EM consult Foster Kennedy syndrome is uncommon. Therefore, a space-occupying lesion should be suspected when there is optic atrophy associated with acute pathology of the other eye. CASE REPORT: A 56-year-old man presented with hemiretinal retinal vein occlusion in his right eye. He had previous optic nerve atrophy in his left eye attributed to.

Foster Kennedy syndrome Radiology Reference Article

Foster Kennedy Syndrome is a paraneoplastic syndrome. It can be caused by any tumor of the frontal lobe .It is characterized by four symptoms : Damage to the optic nerve on the same side as the tumor. The only treatment of the condition is to treat the underlying tumor. Community content is available under CC-BY-SA unless otherwise noted Anosmia, also known as smell blindness, is the loss of the ability to detect one or more smells. Anosmia may be temporary or permanent. It differs from hyposmia which is a decreased sensitivity to some or all smells.. Anosmia can be due to a number of factors, including an inflammation of the nasal mucosa, blockage of nasal passages or a destruction of one temporal lobe. Inflammation is due to. Anosmia (pronounced / æ n ˈ ɒ z m i ə /) is a lack of functioning olfaction, or in other words, an inability to perceive odors.Anosmia may be temporary but traumatic anosmia can be permanent. Anosmia is not due to any inflammation of the nasal mucosa; blockage of nasal passages or a destruction of one temporal lobe Contents. Although Foster Kennedy syndrome is sometimes called Kennedy syndrome, [2] it should not be confused with Kennedy disease, or spinal and bulbar muscular atrophy, which is named after William R. Kennedy. Pseudo-Foster Kennedy syndrome is defined as one-sided optic atrophy with papilledema in the other eye but with the absence of a mass Not Valid for Submission. 377.04 is a legacy non-billable code used to specify a medical diagnosis of foster-kennedy syndrome. This code was replaced on September 30, 2015 by its ICD-10 equivalent

Diagnostic Pitfalls of Pseudo-Foster Kennedy Syndrome - A Case Report To the outpatient facility of the Department of Ophthalmology, Faculty Hospital Brno, Czech Republic, E.U., was in June 2013 referred a 24 years old man with the suspicion of Foster Kennedy syndrome Foster Kennedy syndrome: ( ken'ĕ-dē ), ipsilateral optic atrophy with central scotoma and contralateral choked disc or papilledema, caused by a meningioma of the ipsilateral optic nerve. Synonym(s): Foster Kennedy syndrome Foster-Kennedy Syndrome Add Neural-Optical Lesion Add Optic Disc Disorders Add Optic Disk Disorders Add Optic Nerve Diseases Add Optic Neuropathy Add Second Cranial Nerve Diseases Add Pharm Action Registry Number CAS Type 1 Name NLM Classification # WW 280 Previous Indexing Optic Nerve (1966-1975).

Pseudo-Foster Kennedy syndrome - Retina Image Bank