The authors experienced a case of secondary glaucoma combined with mesodermal dysgenesis of anterior segment, which disclosed extensive peripheral iridocorneal adhesion of congenital origin while his fellow eye revealed a sclerocornea. This case is extremely rare and entirely different from the previously reported Axenfeld's and Rieger's anomalies. We report this interesting case with brief review of the literatures.
Glaucoma* ; Mesoderm*

Klippel-Feil syndrome(KFS) consists of short neck, low posterior hairline and restriction of motion of the neck due to fusion of cervical vertebrae. The typical disorder results from a failure of the normal segmentation of mesodermal somites during 3-8 weeks of gestation. In 1912, the first complete clinical description of this syndrome was given by Klippel and Feil. Feil reported additional cases in 1919 and distinguished between three morphologic groups. The incidence of KFS has been estimated to be approximately 1 : 40,000-42,000 births. A slight female predilection has been noted. Although the disorder is sporadic, there are examples of familial occurrence; how ever, no clear mechanism of inheritance has been accepted. Since the disturbance producing a short neck occurs early in embryogenesis, defects in other organ systems may occur at the same time. Common musculoskeletal anomalies that accompany KFS include scoliosis, as well as Sprengel's deformity in as many as one-third of cases. Neurologic, cardiovascular, and urinary tract anomalies are associated with KPS. We report a case of Klippel-Feil syndrome with associates anomalies include Sprengel's deformity.
Cervical Vertebrae ; Congenital Abnormalities ; Embryonic Development ; Female ; Humans ; Incidence ; Klippel-Feil Syndrome* ; Mesoderm ; Neck ; Parturition ; Pregnancy ; Scoliosis ; Somites ; Urinary Tract ; Wills

The distribution of fibronectin and laminin in early chick embryos has been studied by immunohistochemical method. Fibronectin was detected not only at the basement membranes of neural tube, dorsal aortae and somites but also at the entire mesenchyme area. But laminin only appeared at the basement membranes. During the development of chick embryo, the distribution pattern of these glycoproteins was not changed but showed strong intensity of staining. The dorsal aorta of a 2-day-old chick embryo had several layer of fibronectin-producing cells, but was devoid of laminin. Laminin expression commenced faintly after Day 3. In the brain capillary wall, fibronectin was distributed but laminin was not at Day 10. In the cardiac jelly, fibronectin was detected as thin dotted strands but laminin was not expressed at Day 2. Along the endocardium, fibronectin was detected but laminin was not found. After Day 3, fibronectin was found as increased in endocardium, myocardium and cardiac jelly, whereas laminin expression commenced. Cushion mesenchymal cell migration and development of myocardial trabeculae were inhibited by antifibronectin injected in the cardiac jelly but not anti-laminin. Conclusively, this study suggests that fibronectin and laminin are glycoproteins in the extracellular matrix but there is a difference between their distributions. Cushion mesenchymal cell migration from endocardium and development of trabeculae in chick embryonic heart are inhibited by anti-fibronectin. This result suggests that fibronectin is a `stepping stone` for the embryonic migrating cells and triggers cell migration. But laminin may not serve as a matrix for cell migration.
Animals ; Aorta ; Basement Membrane ; Brain ; Capillaries ; Cell Movement ; Chick Embryo* ; Endocardium ; Extracellular Matrix ; Fibronectins* ; Glycoproteins ; Heart ; Laminin* ; Mesoderm ; Myocardium ; Neural Tube ; Somites

Persistent pupillary membrane ia a congenital anomaly which waa resulted from incomplete atrophy of the fetal vascular arcades and its associated mesodermal tissue derived from the primitive annular vessels. Authors experienced a case (female, 17 years old) of thick persistent pupillary membrane of both eyes which were required complete removal of these membranes under operating microscope. Her corrected vision has improved up to 0.5 (Rt. eye) from 0.1 and 0.7 (Lt eye) from 0.2 without diplopia after operation.
Atrophy ; Diplopia ; Membranes* ; Mesoderm

Primary tumors of the ureter are usually malignant and rare, a few are benign. Benign tumors arising from mesoderm are especially rare. But, recently the incidence rate was progressively increased due to developed methods of diagnostic procedures. We herein report a case of ureteral polyp in the left ureteropelvic junction with a brief review of literatures.
Incidence ; Mesoderm ; Polyps* ; Ureter*

Congenital mesoblastic nephroma is a slow-growing tumor considered to originate from renal mesenchyme and usually discovered before the age of 6 months. The tumor is almost invariably benign but has been mistaken for Wilms` tumor and unnecessarily overtreated. We report a case of congenital mesoblastic nephroma in 2 months aged infant.
Humans ; Infant ; Mesoderm ; Nephroma, Mesoblastic*

Osteogenic sarcoma arise from primitive bone forming mesenchyme which is transformed into neoplastic osteoid and bone. Most osteogenic sarcomas originate in long bone, only rarely do they occur as primary tumor of the spine. A case is presented in which a patient who had suffered from paraplegia and self voiding difficulty. It was diagnosed as osteogenic sarcoma of the 5th thoracic spine which was operated and confirmed by microscopically, and is discussed with a brief review of the literatures.
Humans ; Mesoderm ; Osteosarcoma* ; Paraplegia* ; Spine*

Seminal vesicle cysts combined with ipsilateral renal agenesis represent a rare urologic anomaly. This urogenital malformation is explained as a developmental failure in the same mesodermal region. We report a case of seminal vesicle cyst, ipsilateral dilated ureter and renal agenesis which was treated by surgical excision. And we searched the literature to review the clinical presentation, diagnosis and treatment options of this anomaly.
Diagnosis ; Mesoderm ; Seminal Vesicles* ; Ureter*

Neurofibromatosis(von Reckling hausen's disease) is a congenital heredofamilial disorderresulting from dysplasia of neuroectodermal and mesodermal tissues. It is characterized by developmental anormaly, pigmentary skin lesions and multiple tumors derived from the Schwannian cells of the peripheral and sensory nerve. The authors have experienced two cases of Neurofibromatosis. which is clinically diagnosed. and confirmed by histopathological examination. It was reviewed clinically with the literature.
Mesoderm ; Neural Plate ; Neurofibromatoses* ; Skin

Fibrous hamartoma of infancy (FHI) is a rare benign soft tissue tumor that is composed of an organoid pattern of fibrous tissue and primitive mesenchyme and adipose tissue. The majority of cases of fibrous hamartoma of infancy occur within the first year of life as a single painless subcutaneous nodule. We experienced and report on an uncommon case of protruding fibrous hamartoma of infancy in an 1-year-old girl.
Adipose Tissue ; Hamartoma ; Mesoderm ; Organoids