Monocular Vertical Nystagmus as an Initial Sign of Chiasmal Glioma

1979 ◽  
Vol 87 (1) ◽  
pp. 87-90 ◽  
Author(s):  
Joel A. Schulman ◽  
William T. Shults ◽  
J. Mcandrew Jones
2011 ◽  
Vol 42 (S 01) ◽  
Author(s):  
V Haug ◽  
M von Rhein ◽  
K Frauenknecht ◽  
J Faber ◽  
B Reitter

2020 ◽  
Vol 267 (10) ◽  
pp. 2865-2870
Author(s):  
Torstein R. Meling ◽  
Aria Nouri ◽  
Adrien May ◽  
Nils Guinand ◽  
Maria Isabel Vargas ◽  
...  

Abstract Introduction CNS cavernomas are a type of raspberry-shaped vascular malformations that are typically asymptomatic, but can result in haemorrhage, neurological injury, and seizures. Here, we present a rare case of a brainstem cavernoma that was surgically resected whereafter an upbeat nystagmus presented postoperatively. Case report A 42-year old man presented with sudden-onset nausea, vomiting, vertigo, blurred vision, marked imbalance and difficulty swallowing. Neurological evaluation showed bilateral ataxia, generalized hyperreflexia with left-sided predominance, predominantly horizontal gaze evoked nystagmus on right and left gaze, slight left labial asymmetry, uvula deviation to the right, and tongue deviation to the left. MRI demonstrated a 13-mm cavernoma with haemorrhage and oedema in the medulla oblongata. Surgery was performed via a minimal-invasive, midline approach. Complete excision was confirmed on postoperative MRI. The patient recovered well and became almost neurologically intact. However, he complained of mainly vertical oscillopsia. The videonystagmography revealed a new-onset spontaneous upbeat nystagmus in all gaze directions, not suppressed by fixation. An injury of the rarely described intercalatus nucleus/nucleus of Roller is thought to be the cause. Conclusion Upbeat nystagmus can be related to several lesions of the brainstem, including the medial longitudinal fasciculus, the pons, and the dorsal medulla. To our knowledge, this is the first case of an iatrogenic lesion of the nucleus intercalatus/nucleus of Roller resulting in an upbeat vertical nystagmus. For neurologists, it is important to be aware of the function of this nucleus for assessment of clinical manifestations due to lesions within this region.


1975 ◽  
Vol 80 (1) ◽  
pp. 151-152 ◽  
Author(s):  
Simmons Lessell ◽  
Philip A. Wolf ◽  
David Chronley

2016 ◽  
Vol 20 (3) ◽  
pp. 259-262 ◽  
Author(s):  
Ilya Shoimer ◽  
Nicola Wright ◽  
Richard M. Haber

Primary immunodeficiency disorders, such as ataxia-telangiectasia (A-T), may rarely be associated with cutaneous granulomas without an identifiable infection. The authors report a case of a 3-year-old boy with A-T who presented with two persistent ulcerated erythematous nodules. Histopathology was consistent with a granulomatous process secondary to A-T, without an infectious origin. Partial improvement was noted with clobetasol propionate 0.05% cream applied twice daily under occlusion. Of note, the presence of multiple noninfectious granulomas in a child may be the initial sign of an immune deficiency and should alert the astute clinician to investigate for an underlying primary immunodeficiency. Herein, the authors discuss the associations of noninfectious granulomas and primary immunodeficiency disorders and present management options for these difficult-to-treat lesions.


Author(s):  
Ida Sofie Grønningsæter ◽  
Aymen Bushra Ahmed ◽  
Nils Vetti ◽  
Silje Johansen ◽  
Øystein Bruserud ◽  
...  

The increasing use of radiological examination, especially magnetic resonance imaging (MRI), will probably increase the risk of unintended discovery of bone marrow abnormalities in patients where a hematologic disease would not be expected. In this paper we present four patients with different hematologic malignancies of nonplasma cell types. In all patients the MRI bone marrow abnormalities represent an initial presentation of the disease. These case reports illustrate the importance of a careful diagnostic follow-up without delay of patients with MRI bone marrow abnormalities, because such abnormalities can represent the first sign of both acute promyelocytic leukemia as well as other variants of acute leukemia.


Author(s):  
Gilles Jadd Hoilat ◽  
Abinash Subedi ◽  
Mohamad Fekredeen Ayas ◽  
Nuri Ozden

Extraintestinal manifestations of Crohn's disease sometimes occur and can present prior to intestinal symptoms. Ocular manifestations of Crohn's disease are considered rare, with orbital myositis an even rarer manifestation with only a handful of cases reported in the literature. We present the case of a young woman who was diagnosed with orbital myositis, which was initially attributed to pseudotumor cerebri after an extensive negative work-up. Months later, the patient presented with haematochezia, and was subsequently diagnosed with Crohn's disease.


1997 ◽  
Vol 150 ◽  
pp. S329
Author(s):  
M.B. Seijas ◽  
J.C. Maiques ◽  
R. Ferraro ◽  
L.A. Pliego ◽  
M.L. Arrébola ◽  
...  

PEDIATRICS ◽  
1993 ◽  
Vol 91 (1) ◽  
pp. 153-154
Author(s):  
PETER C. ROWE ◽  
JOHN P. GEARHART

The early identification and surgical correction of urachal anomalies helps to avoid potentially serious sequelae, including infection, rupture of urachal cysts into the peritoneal cavity, and neoplastic change in adult life.1-5 Retraction of the umbilicus during urination has not been described as a physical finding in those with urachal anomalies, but it was an important clinical clue in the patient we describe below. PATIENT REPORT A 12-year-old boy complained of pain at the umbilicus, beginning just after he started to urinate and persisting until approximately 30 seconds after he had finished voiding. The pain had begun abruptly 3 days earlier. It caused him to bend forward and was accompanied by retraction of the umbilicus.


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