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Articles de revues sur le sujet « Cystic angiomatosis »

Auteur : Grafiati

Publié le 7 juin 2025

Mis à jour le 2 août 2025

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1

Clayer, Mark. "Skeletal Angiomatosis in Association with Gastro-Intestinal Angiodysplasia and Paraproteinemia: A Case Report." Journal of Orthopaedic Surgery 10, no. 1 (2002): 85–88. http://dx.doi.org/10.1177/230949900201000115.

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Skeletal-extraskeletal angiomatosis is defined as a benign vascular proliferation involving the medullary cavity of bone and at least one other type of tissue. It has also been known as cystic angiomatosis in which multiple cystic lesions are scattered diffusely throughout the skeleton often with similar angiomatous changes in other tissues, usually the spleen. A case of skeletal angiomatosis in association with gastro-intestinal angiodysplasia and paraproteinemia is reported.

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Lateur, L., C. J. Simoens, S. Gryspeerdt, I. Samson, V. Mertens, and B. Van Damme. "Skeletal cystic angiomatosis." Skeletal Radiology 25, no. 1 (1996): 92–95. http://dx.doi.org/10.1007/s002560050042.

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Fleckenstein, J., John T. Milliken, J. S. Lee, and S. J. Ballentine. "Cystic angiomatosis of the bone, liver, and spleen." American Journal of Clinical Pathology 156, Supplement_1 (2021): S125—S126. http://dx.doi.org/10.1093/ajcp/aqab191.268.

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Abstract Introduction/Objective Cystic angiomatosis is a very rare entity characterized by multifocal cystic angiomatous lesions of the skeletal system, occasionally involving visceral organ systems. Clinical presentation and progression are extremely variable. Cases with liver involvement are even rarer, and have been described as invariably fatal. The pathogenesis of this disorder is poorly understood, and no treatments are currently available. Methods/Case Report A 24 year old man with history of polysubstance abuse and untreated hepatitis C presented with acute abdominal pain. Imaging reve

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Mohan, Sandeep, Rahul Krishnan, Sernam Kuttiyil, S. Archa, Hamdi Nizar Ahamed, and Rashik Ismail. "A Rare Case of Systemic Cystic Angiomatosis in an Elderly Female Initially Misdiagnosed as Vascular Neoplasm: A Case Report and Literature Review." Journal of Orthopaedic Case Reports 15, no. 1 (2025): 8–12. https://doi.org/10.13107/jocr.2025.v15.i01.5104.

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Introduction: Systemic cystic angiomatosis is an exceedingly rare condition characterized by widespread cystic vascular lesions involving multiple organs. Its clinical presentation can be non-specific, often leading to diagnostic challenges. This report discusses the case of a 72-year-old female with a long-standing history of diabetes mellitus who presented with non-specific symptoms, ultimately diagnosed with systemic cystic angiomatosis after an initial misdiagnosis of vascular neoplasia. The role of advanced imaging techniques and a multidisciplinary, individualized management approach is

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Goutoudi, P. C., N. K. Sferopoulos, V. Papavasiliou, and A. Konstantinidis. "Cystic angiomatosis of bone." Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology 81, no. 1 (1996): 89–92. http://dx.doi.org/10.1016/s1079-2104(96)80155-7.

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Boyse, Tedric D., and Jon A. Jacobson. "Case 45: Cystic Angiomatosis." Radiology 223, no. 1 (2002): 164–67. http://dx.doi.org/10.1148/radiol.2231001598.

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International, Journal of Medical Science and Innovative Research (IJMSIR). "Cystic Angiomatosis: A Radiological Dilemma." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 2 (2024): 61–67. https://doi.org/10.5281/zenodo.15378249.

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<strong>Abstract</strong> Cystic angiomatosis is a rare benign disorder with multifocal hemangiomatous or lymphangiomatous lesions of the axial or appendicular skeleton, spleen, liver, and lungs. Patients usually are asymptomatic and are incidentally detected on radiographs. The spectrum clinical presentation may include splenomegaly, hepatomegaly, cystic hygromas or effusions, and pathological fracture depending on the affected area, they may also have neurological symptoms with vertebral localization and skull lesions. This case report illustrates the prompt and accurate diagnosis of cystic

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Najm, Aurélie, Elise Soltner-Neel, Benoît Le Goff, Pascale Guillot, Yves Maugars, and Jean-Marie Berthelot. "Cystic angiomatosis, a heterogeneous condition." Medicine 95, no. 43 (2016): e5213. http://dx.doi.org/10.1097/md.0000000000005213.

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Shivaram, Giridhar M., Reetesh K. Pai, Kevin B. Ireland, and Kathryn J. Stevens. "Temporal progression of skeletal cystic angiomatosis." Skeletal Radiology 36, no. 12 (2007): 1199–204. http://dx.doi.org/10.1007/s00256-007-0378-3.

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REID, A. B., I. L. REID, G. JOHNSON, M. HAMONIC, and P. MAJOR. "Familial Diffuse Cystic Angiomatosis of Bone." Clinical Orthopaedics and Related Research 238 (January 1989): 211–18. http://dx.doi.org/10.1097/00003086-198901000-00031.

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Cohen, M. D., B. Rougraff, and P. Faught. "Cystic angiomatosis of bone: MR findings." Pediatric Radiology 24, no. 4 (1994): 256–57. http://dx.doi.org/10.1007/bf02015448.

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Morrow, Monica, David Berger, and William Thelmo. "Diffuse cystic angiomatosis of the breast." Cancer 62, no. 11 (1988): 2392–96. http://dx.doi.org/10.1002/1097-0142(19881201)62:11<2392::aid-cncr2820621124>3.0.co;2-n.

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Marraoui, W., J. L. Michel, J. L. Kemeny, and M. Soubrier. "Imaging features of systemic cystic angiomatosis." Diagnostic and Interventional Imaging 96, no. 11 (2015): 1211–13. http://dx.doi.org/10.1016/j.diii.2014.08.009.

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14

Ozerov, S. S., N. G. Uskova, A. V. Pshonkin, I. I. Kalinina, D. M. Konovalov, and A. A. Maschan. "Two rare cases of cystic angiomatosis and a literature review." Pediatric Hematology/Oncology and Immunopathology 20, no. 4 (2021): 148–53. http://dx.doi.org/10.24287/1726-1708-2021-20-4-148-153.

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Cystic angiomatosis is a rare disease characterized by disseminated multifocal hemangiomatous and/or lymphangiomatous cystic lesions of the skeleton with possible visceral organ involvement. Only a few dozens of such patients worldwide have been described in the literature. This article presents two case reports of the patients admitted to the D. Rogachev NRMCPHOI with suspected Langerhans cell histiocytosis. The patient’s parents gave their consent to the use of their child’s data, including photographs, for research purposes and in publications. During the investigation, multiple cysts of th

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Kumar, Vivek, Trishala Meghal, Yanyu Helen Sun, and Yiwu Huang. "Systemic Cystic Angiomatosis Mimicking Metastatic Cancer: A Case Report and Review of the Literature." Case Reports in Medicine 2017 (2017): 1–5. http://dx.doi.org/10.1155/2017/5032630.

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Systemic cystic angiomatosis is a rare benign disorder due to the maldeveloped vascular and lymphatic system with less than 50 cases reported in literature so far. We report here a case of systemic cystic angiomatosis (SCA) with multisystem involvement affecting the neck, thyroid, thoracic cavity, and skeletal system. The patient initially presented in her 4th decade of life with isolated lymphangioma in the neck requiring surgery. However, she experienced full-blown manifestations of SCA in her 6th decade which closely mimicked metastatic cancer. The diagnosis of SCA could only be established

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Bauschard, Michael J., Jonathan L. Hatch, Luis Enrique R. Liogier-Weyback, W. Alexander Vandergrift, and Theodore R. McRackan. "Intracranial Complications From Temporal Bone Cystic Angiomatosis." Otology & Neurotology 38, no. 2 (2017): e1-e2. http://dx.doi.org/10.1097/mao.0000000000001294.

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DePalma, Anthony Andrés R., Kartik Shenoy, and Alok D. Sharan. "Cystic Angiomatosis: A Rare Cause of Thoracic Radiculopathy." JBJS Case Connector 4, no. 3 (2014): e55. http://dx.doi.org/10.2106/jbjs.cc.m.00256.

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18

Vanhoenacker, F. M., A. M. De Schepper, H. De Raeve, and Z. Berneman. "Cystic angiomatosis with splenic involvement: unusual MRI findings." European Radiology 13, S6 (2003): L35—L39. http://dx.doi.org/10.1007/s00330-002-1805-4.

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19

Soler, Rafaela, Francisco Pombo, Amelia Bargiela, Jenaro Graña, and Francisco Arnal. "Diffuse skeletal cystic angiomatosis: MR and CT findings." European Journal of Radiology 22, no. 2 (1996): 149–51. http://dx.doi.org/10.1016/0720-048x(95)00733-7.

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20

Morshed, Aliakbar, and Parviz Mohit. "Cystic angiomatosis of the skull presenting with extradural pneumocephalus." Journal of Neurosurgery 72, no. 6 (1990): 968–70. http://dx.doi.org/10.3171/jns.1990.72.6.0968.

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✓ The case is reported of a 40-year-old militiaman who presented 4 days after a blast injury with a huge swelling of the scalp. The bulge was determined to be an air mass collected extradurally via lysis of the air cells of the mastoid bone. Pathological study of the resected bones revealed cystic angiomatosis. The unusual clinical presentation, as well as the rarity of the pathological findings, prompted this report.

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21

Pulido-Zamudio, Tomas, William Orr, and Morley Lertzman. "Cystic Angiomatosis of the Bone Appearing as Intrathoracic Lung Masses." Canadian Respiratory Journal 8, no. 3 (2001): 187–90. http://dx.doi.org/10.1155/2001/753979.

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A rare case of cystic angiomatosis of the bone (CAB) manifesting as bilateral intrathoracic masses is described. In 1996, a 47-year-old woman was referred to the chest clinic at St Boniface Hospital for evaluation of chronic cough, and her chest radiograph showed large, bilateral pleural-based intrathoracic masses. Ten years before, she had been diagnosed with CAB following bone biopsies of her hip and knee. Computed tomography revealed two chest wall masses with internal septations of bone. CAB is a rare, multicentric disease characterized by involvement of the vascular and lymphatic systems,

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Levey, David S., L. M. MacCormack, David J. Sartoris, Parviz Haghighi, Donald Resnick, and Roger Thorne. "Cystic angiomatosis: case report and review of the literature." Skeletal Radiology 25, no. 3 (1996): 287–93. http://dx.doi.org/10.1007/s002560050082.

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Beeram, Ratna Kumari, and Sareen Seelam. "Massive craniofacial cystic angiomatosis and extra-skeletal angiomatosis: A unique case report and brief review of literature." Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology 28, no. 2 (2016): 122–27. http://dx.doi.org/10.1016/j.ajoms.2015.08.008.

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24

Ishida, Tsuyoshi, Howard D. Dorfman, German C. Steiner, and Alex Norman. "Cystic angiomatosis of bone with sclerotic changes mimicking osteoblastic metastases." Skeletal Radiology 23, no. 4 (1994): 247–52. http://dx.doi.org/10.1007/bf02412356.

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25

Marques, Lia, Elisa Vedes, and Miguel Toscano Rico. "Skeletal cystic angiomatosis: A rare cause of unilateral lytic bone lesions." Case Reports in Clinical Medicine 02, no. 07 (2013): 381–85. http://dx.doi.org/10.4236/crcm.2013.27102.

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26

Pavanello, Marco, Gianluca Piatelli, Marcello Ravegnani, et al. "Cystic angiomatosis of the craniocervical junction associated with Chiari I malformation." Child's Nervous System 23, no. 6 (2007): 697–700. http://dx.doi.org/10.1007/s00381-006-0274-5.

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von Knoch, Fabian, Franz Grill, Andreas M. Herneth, et al. "Skeletal cystic angiomatosis with severe hip joint deformation resembling massive osteolysis." Archives of Orthopaedic and Trauma Surgery 121, no. 8 (2001): 485–88. http://dx.doi.org/10.1007/s004020100295.

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Sferopoulos, N. K., D. Anagnostopoulos, and J. K. Webb. "Cystic angiomatosis of bone with massive osteolysis of the cervical spine." European Spine Journal 7, no. 3 (1998): 257–59. http://dx.doi.org/10.1007/s005860050069.

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Porto, Guilherme B. F., Cynthia T. Welsh, M. Imran Chaudry, and Ramin Eskandari. "Cystic angiomatosis skull lesion obliteration with neuroendovascular sclerotherapy as a unique treatment: case report." Journal of Neurosurgery: Pediatrics 26, no. 2 (2020): 145–49. http://dx.doi.org/10.3171/2020.3.peds2045.

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Cystic angiomatosis is a rare bone condition with complex presentation and difficult treatment. Current management strategies have poorly tolerated side effects and a low likelihood of disease eradication. The control of calvarial lesions that are symptomatic usually involves surgical excision and subsequent cranioplasty. This paradigm can present with a risk of morbidity and mortality depending on the anatomy of the lesion. Here, the authors present a novel approach to a difficult-to-treat occipital calvarial lesion directly overlying the transverse sinus, performing a small, partial-thicknes

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Bardeguez, A., M. Chatterjee, M. Tepedino, and B. Sicuranza. "Systemic cystic angiomatosis in pregnancy: A case presentation and review of the literature." American Journal of Obstetrics and Gynecology 163, no. 1 (1990): 42–45. http://dx.doi.org/10.1016/s0002-9378(11)90663-2.

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Yadav, Yogesh Kumar, Gaurav Kumar, Vikas Verma, and Anuj Rastogi. "Cystic angiomatosis: a rare cause of osteolytic lesions and pathological fracture - a case report." Indian Journal of Orthopaedics Surgery 1, no. 2 (2015): 121. http://dx.doi.org/10.5958/2395-1362.2015.00010.9.

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Marcucci, Gemma, Laura Masi, Anna Maria Carossino, et al. "Cystic Bone Angiomatosis: A Case Report Treated with Aminobisphosphonates and Review of the Literature." Calcified Tissue International 93, no. 5 (2013): 462–71. http://dx.doi.org/10.1007/s00223-013-9761-3.

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Markar’yan, Irina V., Natalia V. Yermolova, Nina A. Drukker, Vladimir Y. Mazhugin, Alexander N. Rymasheuski, and Sofia A. Trushina. "Morphological substantiation of pathogenetic therapyof external genital endometriosis." Journal of obstetrics and women's diseases 65, no. 6 (2016): 100–103. http://dx.doi.org/10.17816/jowd656100-103.

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With the help of morphological study examined endometrioid heterotopias and eutopic endometrium in external genital endometriosis. Histological examination of surgical specimens of endometrial cancer were detected in endometrioid heterotopia, in eutopic endometrium occurred glandular-cystic hyperplasia of the proliferative and secretory type. Have been identified in the heterotopias expressed angiomatosis in patients with III-IV stages of endometriosis. It is proved that inflammatory changes in endometrioid heterotopias more pronounced with stage I-II stages of endometriosis, whereas hyalinosi

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Hossein Mortazavi, Seyed, Abbas Khodayari, Arash Khojasteh, et al. "Massive Craniofacial Intraosseous Vascular Malformation Resembling Cystic Angiomatosis: Report of 2 Cases and Review of the Literature." Journal of Oral and Maxillofacial Surgery 69, no. 1 (2011): 204–14. http://dx.doi.org/10.1016/j.joms.2010.07.072.

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Khapchenkova, Daria S., and Ganna S. Senatorova. "PECULIAR FEATURES OF AORTIC WALL STRUCTURE AMONG CHILDREN WITH COARCTATION." Wiadomości Lekarskie 73, no. 4 (2020): 789–91. http://dx.doi.org/10.36740/wlek202004132.

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The aim of the study to evaluate the peculiarities of the aortic wall structure at the place of coarctation. Materials and methods: Studying of the aortic sections removed during operative correction at the place of constriction. 10 children at the age between 1 to 6 months were undergone the operation. Intraoperative aortic biopsy specimens were observed in 10% neutral formalin. Histologic sections were prepared in a conventional way followed by staining them with hematoxylin-eosin. Results: Histological examination in the areas of constriction revealed that the endothelium in all the prepara

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Mahapatra, Ashok, Susama Patra, and Sumit Bansal. "Cystic Angiomatous Meningioma: A Diagnostic Dilemma." Indian Journal of Neurosurgery 05, no. 02 (2016): 106–9. http://dx.doi.org/10.1055/s-0036-1581981.

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Dhingra, Preeti, Naresh Palapalle, Dilroop K. Poyyil, and Rakesh Katna. "Sinonasal angiomatous polyp: a case report." International Journal of Otorhinolaryngology and Head and Neck Surgery 8, no. 12 (2022): 1000. http://dx.doi.org/10.18203/issn.2454-5929.ijohns20223052.

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<p>Sinonasal angiomatous polyp (SAP) is a rare variant of sino-nasal polyp. Sinonasal inflammatory polyps are classified histo-pathologically into 5 types: edematous, glandular, fibrous, cystic and angiomatous. They present with various different patterns and clinical features like epistaxis, nasal discharge, nasal blockage and characterised histo-pathologically by presence of prominent dilated capillary-type blood vessels. It constitutes about 4-5% of all nasal polyps. They usually present as a unilateral, painless, soft, gelatinous, translucent and polypoidal mass in nasal cavity. Thes

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Ichikawa, Jiro, Tomonori Kawasaki, Kojiro Onohara, et al. "Indolent Angiomatoid Fibrous Histiocytoma Mimicking a Benign Cystic Tumor." Diagnostics 15, no. 1 (2025): 115. https://doi.org/10.3390/diagnostics15010115.

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Angiomatoid fibrous histiocytoma (AFH) is a rare intermediate tumor that is often difficult to diagnose radiologically and pathologically. Herein, we report a case of AFH in the knee that was initially misdiagnosed as a cystic lesion. The tumor was first identified eight years earlier during the patient’s initial visit, when plain magnetic resonance imaging (MRI) was performed, leading to a diagnosis of a cystic lesion. At the current visit, the tumor had subsequently enlarged, and pain had appeared. Contrast-enhanced MRI was performed at our hospital, revealing enhancement suggestive of a sol

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Sapra, Akhilesh, Syed Zafar, Vijayalakshmi Gudivada, and Piyush Somani. "Laparoscopic resection of a giant adrenal cyst: a case report." International Surgery Journal 12, no. 7 (2025): 1153–56. https://doi.org/10.18203/2349-2902.isj20251911.

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Giant adrenal cysts, often discovered incidentally, are rare lesions. This case report details a patient who had many symptoms, including nonspecific abdominal distension. Imaging tests showed a large cystic growth that was closely connected to the left adrenal gland. No abnormalities were found in routine laboratory and endocrine function tests. Laparoscopic surgery was used, and the cystic mass was entirely removed. Upon pathological inspection, an endothelial structure with vascular components was found in the cyst wall. After extensive evaluation, the lesion was determined to be an angioma

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Thway, Khin. "Angiomatoid Fibrous Histiocytoma: A Review With Recent Genetic Findings." Archives of Pathology & Laboratory Medicine 132, no. 2 (2008): 273–77. http://dx.doi.org/10.5858/2008-132-273-afharw.

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Abstract Angiomatoid fibrous histiocytoma is a neoplasm of intermediate biologic potential most often arising in the extremities of children and young adults. Its rarity may lead to misdiagnosis as either a reactive lesion or a benign or higher-grade tumor. Originally described as a type of malignant fibrous histiocytoma, its differentiation remains enigmatic, with precise histogenesis still only hypothesized. Its morphology is distinct, as a circumscribed lesion with sheets of bland spindle to ovoid cells, peripheral lymphoplasmacytic infiltrate, and blood-filled cystic cavities, and half of

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Deb, Prabal, Hirdesh Sahni, and HarjinderSingh Bhatoe. "Cystic angiomatous meningioma in the cerebellopontine angle mimicking hemangioblastoma." Journal of Cancer Research and Therapeutics 6, no. 4 (2010): 560. http://dx.doi.org/10.4103/0973-1482.77074.

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Joshi, Anagha R., Kiran Kulkarni, and Ankita U. Shah. "Labrune Syndrome: A Very Rare Association of Leukoencephalopathy, Cerebral Calcifications, and Cysts." Indian Journal of Radiology and Imaging 31, no. 03 (2021): 772–75. http://dx.doi.org/10.1055/s-0041-1736398.

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AbstractLeukoencephalopathy, cerebral calcifications, and cysts (LCC) form a very rare association which is named as “Labrune syndrome” after Labrune who reported the first case in 1996. To the best of our knowledge only eight to 10 cases have been reported in literature to date. We report a case of a 26-year-old male with onset of neurological symptoms in late adolescence (at 19 years of age) and presented with complains of continued seizures for 7 years, giddiness with imbalance, and slowly progressive motor symptoms. MRI brain revealed multiple calcifications in bilateral basal ganglia, cer

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Koletsa, Triantafyllia, Prodromos Hytiroglou, Christos Semoglou, Antonios Drevelegas, and Georgios Karkavelas. "Angiomatoid fibrous histiocytoma with cystic structures of sweat duct origin." Pathology International 57, no. 8 (2007): 513–16. http://dx.doi.org/10.1111/j.1440-1827.2007.02133.x.

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Ghazanfar, Jawaria, Amna Idrees, Muhammad Ali Sheikh, Muhammad Zaeem Khalid, and Amna Ikram. "Angiomatoid Fibrous Histiocytoma: A Rare Cause of Anemia in a Child." Esculapio 18, no. 3 (2022): 395–99. http://dx.doi.org/10.51273/esc22.25183-cr.

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Angiomatoid fibrous histiocytoma (AFH) is a rare soft tissue tumor of intermediate potential and is usually found during first two decades of life. It is located mainly in extremities presents as a painless, slow growing mass with extensive blood supply. Embryologically, it arises from a pluripotent mesenchymal cell. Histologically, the tumor has thick pseudo capsule with chronic inflammatory infiltrates and hemorrhagic cystic areas. We present a case of AFH which caused severe anemia in a child with a non-healing ulcer on the medial aspect of left knee. Multiple blood transfusions, incision a

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Alsaadi, Khaled A., Manar Alwohaib, Karen Pinto, and Rola H. Ali. "Giant cell-rich solitary fibrous tumour of the lacrimal gland with prominent angiomatoid cystic changes and an underlying NAB2ex3-STAT6ex18 fusion." BMJ Case Reports 15, no. 2 (2022): e247141. http://dx.doi.org/10.1136/bcr-2021-247141.

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Giant cell-rich solitary fibrous tumour (GCR-SFT) is a rare variant of SFT with a predilection for the orbital region. Despite its hypervascularity, extensive angiomatoid cystic changes are unusual in GCR-SFT and may pose a diagnostic challenge. A 47-year-old man presented with a right eye proptosis and a protruding tumour of several years’ duration with recently accelerated tumour growth. MRI revealed a cystic-solid heterogeneous mass arising from the lacrimal gland and displacing the globe. A subtotal excision of the mass was performed due to unanticipated hypervascularity and intraoperative

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Ozer, Songul Peltek. "Cutaneous Epithelioid Angiomatous Nodule with Unusual Localization." National Journal of Health Sciences 8, no. 1 (2023): 42–44. http://dx.doi.org/10.21089/njhs.81.0042.

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Abstract: Brenn and Fletcher described cutaneous epithelioid angiomatous nodule (CEAN) as a benign vascular proliferation that was in 2004. It is very rare condition. It is characterized by endothelial cells that have histiocytoid appearance. It is generally found in the dermis or sub cutis and rarely, in visceral organs. Despite the etiology of CEAN is not clear, it is considered as a reactive entity and no association with either infection, trauma or immunosuppression has been described yet. A 76-year-old woman visited hospital for routine examination. The physician noticed an erythematous n

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Thway, Khin, and Cyril Fisher. "Angiomatoid Fibrous Histiocytoma: The Current Status of Pathology and Genetics." Archives of Pathology & Laboratory Medicine 139, no. 5 (2015): 674–82. http://dx.doi.org/10.5858/arpa.2014-0234-ra.

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Context Angiomatoid fibrous histiocytoma (AFH) is a rare soft tissue neoplasm of intermediate biologic potential and uncertain differentiation, most often arising in the superficial extremities of children and young adults. While it has characteristic histologic features of nodular distributions of ovoid and spindle cells with blood-filled cystic cavities and a surrounding dense lymphoplasmacytic infiltrate, there is a significant morphologic spectrum, which coupled with its rarity and lack of specific immunoprofile can make diagnosis challenging. Angiomatoid fibrous histiocytoma is associated

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Lisovaja, Ija, Ivanda Franckevica, and Natalija Vedmedovska. "Large Angiomyxoma of the Umbilical Cord-Uncomplicated Rupture of Tumor Membranes at 32 Weeks of Gestation." Diagnostics 12, no. 6 (2022): 1339. http://dx.doi.org/10.3390/diagnostics12061339.

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Background: When a tumor of the umbilical cord is prenatally visualized, it is possible to propose the diagnosis depending on the sonographic appearance of the tumor. Angiomyxoma of the umbilical cord appears as a complex solid-cystic mass that is made of angiomatous component and myxoid stroma. When the tumor is diagnosed, serial ultrasound and doppler examinations are used to monitor the tumor’s size and the overall fetal well-being including doppler investigations and fetal growth. Angiomyxomas are not associated with fetal chromosomal pathologies. The cases of intrauterine rupture and feta

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Janevska, Vesna, Vlado Janevski, Oliver Stankov, Liljana Spasevska, Slavica Kostadinova-Kunovska, and Julija Zhivadinovik. "Non-Tumor Cystic Lesions of the Adrenal Gland." PRILOZI 36, no. 3 (2015): 51–59. http://dx.doi.org/10.1515/prilozi-2015-0078.

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Abstract Adrenal cystic lesions are uncommon but due to the improved radiologic imaging techniques their appearance seems to increase. Material and Methods: We analyzed the clinical and radiological findings of 10 patients with adrenal cysts and the pathological features of the operative material. Standard dissection procedure and paraffin embedded tissue sections were made, stained by HE and immunohistochemically with CD34, CD 31, Factor 8, Podoplanin, CKWS and AE1/AE3 Results: The mean age of the patients was 40.6 years; female to male ratio was 2.3:1. All the cysts were diagnosed as cystic

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Tas, Betul, Seyda Andac, and Aysel Caglar. "Silhouette Lymphangioma: An Unknown Macular Form of Cutaneous Lymphangioma." Archives of Iranian Medicine 25, no. 7 (2022): 456–59. http://dx.doi.org/10.34172/aim.2022.75.

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Unusual angiomatous or lymphangiomatous vascular malformations are rarely seen. One of them is lymphangioma (LA), which is a rare benign lymphovascular abnormality. LA is usually seen in the types of circumscriptum (or capillary), cavernous and cystic. Here, we report a unique case of LA with a patchy appearance. The patient presented due to unusual symptoms and eccentric clinical manifestation of the lesion. Here, we present a new lymphatic entity which was diagnosed as LA with its clinical, radiological and pathological findings. Written informed consent of the patient was obtained for this

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