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1.
Zhonghua Jie He He Hu Xi Za Zhi ; 47(7): 658-662, 2024 Jul 12.
Artículo en Zh | MEDLINE | ID: mdl-38955752

RESUMEN

Malignant peripheral nerve sheath tumor (MPNST) frequently metastasizes to the lungs, although pleural metastasis is rare. This article reported a case of pleural metastasis of MPNST. The patient was a young man who presented with 1 week of shortness of breath with dry cough. He had a history of malignant peripheral nerve sheath tumor. The patient was diagnosed with MPNST pleural metastasis after a thoracoscopic pleural biopsy, which revealed short spindle cell hyperplasia, immunohistochemical staining for S-100(+), SOX-10(+), Ki-67(+) with a positive index of 20%, and H3K27Me3(-) in the pleural pathology.


Asunto(s)
Neoplasias de la Vaina del Nervio , Neoplasias Pleurales , Humanos , Masculino , Neoplasias Pleurales/secundario , Neoplasias Pleurales/patología , Neoplasias de la Vaina del Nervio/patología , Neoplasias de la Vaina del Nervio/secundario , Neoplasias de la Vaina del Nervio/diagnóstico , Adulto
2.
Zhonghua Jie He He Hu Xi Za Zhi ; 45(1): 53-58, 2022 Jan 12.
Artículo en Zh | MEDLINE | ID: mdl-35000306

RESUMEN

Objective: To improve the understanding of clinical manifestations, imaging findings, diagnosis and treatment of surfactant protein C gene (SFTPC) mutation associated with familial interstitial lung disease in adults. Methods: Two cases of adult SFTPC gene mutation associated with familial interstitial lung disease diagnosed in the Affiliated Hospital of Medical School of Ningbo University were analyzed retrospectively, and the literature was reviewed. The literatures were retrieved with "family interstitial lung disease" "SFTPC gene" "surface protein C gene" "SFTPC gene mutation associated with familial international lung disease" and "surface protein C gene mutation associated with familial international lung disease" in PubMed, Embase, Ovid, Wanfang database and China National Knowledge Infrastructure (CNKI). Results: There were two patients with familial interstitial lung diseases(one male and one female) with an average age of 27.5 years. Ⅱ-2 patient had symptoms of dry cough and shortness of breath, and Ⅱ-1 patient had no symptoms. There were multiple cysts and fine reticular shadows in both cases. Ⅱ-2 patient had multiple ground glass opacities in both lower lungs. TheⅡ-2 patient was diagnosed with usual interstitial pneumonia (UIP) by transbronchial lung cryobiopsy. A total of 35 patients were included in this literature review, including 20 males, with an average age of 33.5 years. Of all the patients, the clinical symptoms were described in 30 patients. The main manifestations were shortness of breath (22/30), dry cough (18/30), clubbing finger (12/30), and 30% (9/30) of them were found by chest computerized tomography (CT) without symptoms. There were 17 cases with detailed description of chest CT imaging. The most common chest CT findings were multiple intralobular reticular opacities (17/17), multiple cysts (12/17) and ground glass opacities (7/17). The main histopathological pattern was UIP (24/26). Conclusions: The main clinical manifestations of SFTPC gene mutation associated with familial interstitial lung disease in adults are shortness of breath, dry cough and clubbing fingers. The main manifestations are multiple cysts and intralobular reticular opacities in combination with multiple ground glass opacities. There is no specific drug in the treatment at present and early treatment with hydroxychloroquine may have better curative effect. When the imaging findings show multiple cysts and intralobular reticular opacities in combination with multiple ground glass opacities, especially the age of onset is less than 50 years old, this disease should be considered.


Asunto(s)
Enfermedades Pulmonares Intersticiales , Proteína C , Adulto , Femenino , Humanos , Pulmón , Enfermedades Pulmonares Intersticiales/diagnóstico por imagen , Enfermedades Pulmonares Intersticiales/genética , Masculino , Persona de Mediana Edad , Mutación , Proteína C Asociada a Surfactante Pulmonar , Estudios Retrospectivos , Tensoactivos
3.
J Intern Med ; 282(1): 5-23, 2017 07.
Artículo en Inglés | MEDLINE | ID: mdl-28155242

RESUMEN

Sensory neurons in the gastrointestinal tract have multifaceted roles in maintaining homeostasis, detecting danger and initiating protective responses. The gastrointestinal tract is innervated by three types of sensory neurons: dorsal root ganglia, nodose/jugular ganglia and intrinsic primary afferent neurons. Here, we examine how these distinct sensory neurons and their signal transducers participate in regulating gastrointestinal inflammation and host defence. Sensory neurons are equipped with molecular sensors that enable neuronal detection of diverse environmental signals including thermal and mechanical stimuli, inflammatory mediators and tissue damage. Emerging evidence shows that sensory neurons participate in host-microbe interactions. Sensory neurons are able to detect pathogenic and commensal bacteria through specific metabolites, cell-wall components, and toxins. Here, we review recent work on the mechanisms of bacterial detection by distinct subtypes of gut-innervating sensory neurons. Upon activation, sensory neurons communicate to the immune system to modulate tissue inflammation through antidromic signalling and efferent neural circuits. We discuss how this neuro-immune regulation is orchestrated through transient receptor potential ion channels and sensory neuropeptides including substance P, calcitonin gene-related peptide, vasoactive intestinal peptide and pituitary adenylate cyclase-activating polypeptide. Recent studies also highlight a role for sensory neurons in regulating host defence against enteric bacterial pathogens including Salmonella typhimurium, Citrobacter rodentium and enterotoxigenic Escherichia coli. Understanding how sensory neurons respond to gastrointestinal flora and communicate with immune cells to regulate host defence enhances our knowledge of host physiology and may form the basis for new approaches to treat gastrointestinal diseases.


Asunto(s)
Gastroenteritis/fisiopatología , Tracto Gastrointestinal/inervación , Células Receptoras Sensoriales/fisiología , Fenómenos Fisiológicos Bacterianos , Gastroenteritis/inmunología , Gastroenteritis/microbiología , Humanos , Canales Iónicos/fisiología , Neuropéptidos/fisiología
4.
J Clin Neurosci ; 5(3): 338-9, 1998 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-18639044

RESUMEN

This case illustrates the need to recognize a high cervical cord injury as a cause for bi-brachial weakness with intact bi-crural power, a pattern termed aptly by Sage as 'man in the barrel' syndrome. The patient who had an undiagnosed Klippel-Feil deformity had incurred his cervical injury after a collapse.

5.
Med Law ; 16(2): 253-67, 1997.
Artículo en Inglés | MEDLINE | ID: mdl-9212618

RESUMEN

We examined the licensing of drivers with conditions likely to endanger the public in a State in which doctors are obliged to notify the licensing authority. During 1991, 1460 medically endorsed licenses were cancelled. A sample of 245, including all 49 with epilepsy were mostly voluntary, the twenty exceptions with retained files being drivers with epilepsy. In the same period, 115 traffic accidents were attributed to illness, with the only four (4) investigated by the licensing authority being those with licenses endorsed "epilepsy" where a seizure was responsible. Compulsory notification appeared to result in the identification of epilepsy as the important medical reason for controlling licenses, but failed to recognise sleep disorders or alcoholism, both more significant causes of traffic accidents. In those accidents attributed to illness, almost no action was taken to review the medical fitness of drivers, suggesting a reliance on doctors rather than police or road safety authorities.


Asunto(s)
Conducción de Automóvil/legislación & jurisprudencia , Notificación de Enfermedades/legislación & jurisprudencia , Epilepsia , Accidentes de Tránsito/legislación & jurisprudencia , Accidentes de Tránsito/prevención & control , Evaluación de la Discapacidad , Ética Médica , Humanos , Concesión de Licencias/legislación & jurisprudencia , Australia del Sur
6.
Oncology ; 45(4): 331-5, 1988.
Artículo en Inglés | MEDLINE | ID: mdl-3387038

RESUMEN

The ability of dexamethasone (DM) to slow the growth of B16 melanoma in C57B1 mice was confirmed. Inhibition was dose-related and was demonstrated in the use of established tumours as well as initial transplants. Although glucocorticoid receptors (GR) were present in cultured tumour cells, DM did not reduce growth of B16 in vitro, even at high concentration. This dissociation of effect on growth in vivo and in vitro suggests that DM slows B16 tumour growth in vivo by mechanisms other than GR-mediated inhibition of tumour cells.


Asunto(s)
Dexametasona/farmacología , Melanoma/patología , Receptores de Glucocorticoides/metabolismo , Animales , División Celular/efectos de los fármacos , Línea Celular , Melanoma/metabolismo , Ratones , Ratones Endogámicos C57BL , Trasplante de Neoplasias , Receptores de Glucocorticoides/efectos de los fármacos , Células Tumorales Cultivadas/efectos de los fármacos
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