胸腺发育不全的临床病理研究 - Suppr

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超能文献

Clinico-pathological study of thymic dysplasia.

作者信息

Berry C L, Thompson E N

出版信息

Arch Dis Child. 1968 Oct;43(231):579-84. doi: 10.1136/adc.43.231.579.

DOI:10.1136/adc.43.231.579

PMID:4177044

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2020022/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4ea/2020022/14207e322d76/archdisch01560-0079-a.jpg

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Clinico-pathological study of thymic dysplasia.胸腺发育不全的临床病理研究

Arch Dis Child. 1968 Oct;43(231):579-84. doi: 10.1136/adc.43.231.579.

Thymic alymphoplasia, monoclonal gammopathy, and Pneumocystis carinii pneumonia in an infant.一名婴儿的胸腺无淋巴细胞形成、单克隆丙种球蛋白病和卡氏肺孢子虫肺炎。

Arch Dis Child. 1968 Aug;43(230):444-50. doi: 10.1136/adc.43.230.444.

Thymic alymphoplasia and dysgammaglobulinemia type I. Clinical, immunological, and pathological studies of one case.

J Pediatr. 1969 Jul;75(1):95-103. doi: 10.1016/s0022-3476(69)80106-x.

Selective immunoglobulin deficiency associated with thymic alymphoplasia.

Pediatrics. 1967 Apr;39(4):506-15.

Thymic dysplasia ("Swiss agammaglobulinemia"). I. Graft versus host reaction following bone-marrow transfusion.胸腺发育不全（“瑞士型无丙种球蛋白血症”）。一、骨髓输血后的移植物抗宿主反应。

J Pediatr. 1967 May;70(5):730-6. doi: 10.1016/s0022-3476(67)80323-8.

Thymic dysplasia with immunological deficiency. Report of two unusual cases.胸腺发育不全伴免疫缺陷。两例罕见病例报告。

Acta Pathol Microbiol Scand. 1969;76(3):349-60.

An autopsy case of lymphopenic hypogammaglobulinemia.

Acta Pathol Jpn. 1967 Nov;17(4):465-73. doi: 10.1111/j.1440-1827.1967.tb02736.x.

A case of thymic alymphoplasia with synthesis of IgM globulin.

Acta Paediatr Scand. 1967 Jul;56(4):430-5. doi: 10.1111/j.1651-2227.1967.tb15402.x.

Lymphopenic forms of congenital immunologic deficiency diseases.先天性免疫缺陷疾病的淋巴细胞减少型

Medicine (Baltimore). 1968 May;47(3):201-26. doi: 10.1097/00005792-196805000-00002.

[Thymus dysplasia].[胸腺发育不全]

Orv Hetil. 1971 Nov 28;112(48):2893-5.

引用本文的文献

Rubella virus chronic inflammatory disease and other unusual viral phenotypes in inborn errors of immunity.风疹病毒慢性炎症性疾病和其他先天性免疫缺陷中的异常病毒表型。

Immunol Rev. 2024 Mar;322(1):113-137. doi: 10.1111/imr.13290. Epub 2023 Nov 27.

An unusual case of metaphyseal chondrodysplasia with an abnormal perilacunar matrix associated with agranulocytosis and hypoplasia of the thymus.一例罕见的干骺端软骨发育异常病例，伴有异常的陷窝周围基质，与粒细胞缺乏症和胸腺发育不全相关。

Virchows Arch A Pathol Anat Histol. 1981;391(3):275-89. doi: 10.1007/BF00709160.

Treatment of severe combined immunodeficiency by transplantation.通过移植治疗重症联合免疫缺陷。

Blut. 1981 Mar;42(3):137-48. doi: 10.1007/BF01026383.

Candida septicaemia.念珠菌败血症

Br Med J. 1969 Mar 1;1(5643):577. doi: 10.1136/bmj.1.5643.577.

Histopathological findings in the combined immunity-deficiency syndrome.联合免疫缺陷综合征的组织病理学发现。

J Clin Pathol. 1970 Apr;23(3):193-202. doi: 10.1136/jcp.23.3.193.

Chronic encephalitis in children with severe immuno-deficiency.重度免疫缺陷儿童的慢性脑炎

Acta Neuropathol. 1971;19(3):234-41. doi: 10.1007/BF00684600.

In vitro lymphocyte response in some immunity deficiency diseases and in intrauterine virus infections.某些免疫缺陷疾病及宫内病毒感染中的体外淋巴细胞反应。

Proc R Soc Med. 1970 Apr;63(4):351-4. doi: 10.1177/003591577006300410.

[Incomplete, combined hereditary immunodeficiency with generalized tuberculosis after BCG-vaccination from bacille Calmette Guérin (author's transl)].[卡介苗接种后发生不完全性、合并遗传性免疫缺陷及播散性结核病（作者译）]

Virchows Arch A Pathol Anat Histol. 1975;366(4):341-51. doi: 10.1007/BF00433893.

Cell-mediated immunity and its role in resistance to infection.细胞介导的免疫及其在抗感染中的作用。

West J Med. 1977 Jan;126(1):14-31.

本文引用的文献

[Essential lymphocytophthisis; new clinical aspect of infant pathology].[原发性淋巴细胞消耗症；婴儿病理学的新临床方面]

Ann Paediatr. 1950 Jul-Aug;175(1-2):1-32.

[HEREDITARY THYMIC HYPOPLASIA: ITS PLACE AND RESPONSIBILITY IN A CASE OF LYMPHOCYTIC, NORMOPLASMOCYTIC AND NORMOGLOBULINEMIC APLASIA IN AN INFANT].[遗传性胸腺发育不全：在一名婴儿淋巴细胞、正常浆细胞和正常球蛋白血症性再生障碍性贫血病例中的地位及作用]

Arch Fr Pediatr. 1964 Oct;21:897-920.

ATAXIA-TELANGIECTASIA. ITS ASSOCIATION WITH A DEFECTIVE THYMUS, IMMUNOLOGICAL-DEFICIENCY DISEASE, AND MALIGNANCY.共济失调毛细血管扩张症。其与胸腺缺陷、免疫缺陷病及恶性肿瘤的关联。

Lancet. 1964 May 30;1(7344):1189-93. doi: 10.1016/s0140-6736(64)91209-7.

DYSTROPHIC CHANGES ASSOCIATED WITH LEPRECHAUNISM IN A MALE INFANT.一名男婴中与拉普-莱伦侏儒症相关的营养不良性改变。

Arch Dis Child. 1963 Oct;38(201):530-5. doi: 10.1136/adc.38.201.530.

Estimation of eight serum proteins by a gel diffusion precipitin technique.采用凝胶扩散沉淀技术对八种血清蛋白进行测定。

J Lab Clin Med. 1962 May;59:859-70.

Reticular dysgenesia.网状细胞发育不全

Lancet. 1959 Dec 19;2(7112):1123-5. doi: 10.1016/s0140-6736(59)90105-9.

[Familial lymphopenia with agammaglobulinemia & severe moniliasis: the essential lymphocytophthisis as a special form of early childhood agammaglobulinemia].[伴有无丙种球蛋白血症和严重念珠菌病的家族性淋巴细胞减少症：作为幼儿期无丙种球蛋白血症一种特殊形式的原发性淋巴细胞消耗症]

Helv Paediatr Acta. 1958 Oct;13(4):313-38.

Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea.系谱显示一种X连锁隐性疾病，其特征为耳漏、湿疹样皮炎和血性腹泻。

Pediatrics. 1954 Feb;13(2):133-9.

Thymic lymphocytophthisis with terminal aplastic anaemia.胸腺淋巴细胞消耗症伴终末期再生障碍性贫血。

Proc R Soc Med. 1967 Sep;60(9):895-7. doi: 10.1177/003591576706000932.

Thymic alymphoplasia.胸腺淋巴细胞发育不全

Arch Dis Child. 1967 Feb;42(221):40-54. doi: 10.1136/adc.42.221.40.

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