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Journal articles on the topic 'Leiomyomatose'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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1

Schumacher, A., G. Saile, H. Brühwiler, and K. Lüscher. "Intravenöse Leiomyomatose." Geburtshilfe und Frauenheilkunde 55, no. 10 (1995): 602–4. http://dx.doi.org/10.1055/s-2007-1023533.

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2

Kommoss, F., T. Ebel, J. Drusenheimer, et al. "Die intravenöse Leiomyomatose." Der Pathologe 40, no. 1 (2019): 80–84. http://dx.doi.org/10.1007/s00292-019-0566-7.

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3

Padberg, B. C., A. Emmermann, C. Zornig, M. Germer, and S. Schröder. "Leiomyomatose des Rektums." Der Pathologe 28, no. 2 (2007): 161–65. http://dx.doi.org/10.1007/s00292-007-0898-6.

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4

Braun, S. A., S. Hanneken, J. Reifenberger, D. Helbig, and J. Frank. "Hereditäre kutane Leiomyomatose." Der Hautarzt 63, no. 4 (2012): 276–78. http://dx.doi.org/10.1007/s00105-012-2357-4.

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5

Acid, S., S. Marciano-Chagnaud, P. Kbaier, et al. "AGF14 Leiomyomatose peritoneale disseminee." Journal de Radiologie 87, no. 10 (2006): 1440. http://dx.doi.org/10.1016/s0221-0363(06)87509-8.

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6

Bergmann, M., B. Seelbach-Göbel, and H. Müller-Hermelink. "Intravenöse Leiomyomatose des Uterus." Geburtshilfe und Frauenheilkunde 51, no. 11 (1991): 942–44. http://dx.doi.org/10.1055/s-2008-1026241.

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7

Scharlau, L.-L. L.-L., J. Scharlau, Cl Mathuis, and C.-N. C.-N. Schremmer. "Diffuse peritoneale Leiomyomatose - Eine klinische Fallstudie - Diffuse Peritoneal Leiomyomatosis: A Case Report -." Geburtshilfe und Frauenheilkunde 60, no. 4 (2000): 225–28. http://dx.doi.org/10.1055/s-2000-10014.

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8

Versini, M., PY Jeandel, A. Rahili, et al. "Leiomyomatose surrénalienne : une localisation exceptionnelle." La Revue de Médecine Interne 32 (June 2011): S179—S180. http://dx.doi.org/10.1016/j.revmed.2011.03.305.

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9

Kruczynski, D., E. Merz, Th Beck, et al. "Minimal invasive Therapie bei peritonealer Leiomyomatose." Geburtshilfe und Frauenheilkunde 54, no. 03 (1994): 181–83. http://dx.doi.org/10.1055/s-2007-1023578.

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10

Werthemann, A., B. Unger, H. Lobeck, and H. Wenisch. "Die verzögerte Ösophagusresektion bei diffuser Leiomyomatose." Zentralblatt für Chirurgie 136, no. 03 (2010): 282–83. http://dx.doi.org/10.1055/s-0030-1247322.

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11

Peters, A. S., M. S. Bischoff, J. Weitz, et al. "Die intravenöse Leiomyomatose – eine seltene Tumorentität." Gefässchirurgie 17, no. 5 (2012): 374–77. http://dx.doi.org/10.1007/s00772-012-0999-2.

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12

Henschen, St, M. Gronewold, Ch Thomssen, L. Riethdorf, and F. Jänicke. "Kasuistik einer Leiomyomatose pelviner Lymphknoten unter Östrogensubstitution." Geburtshilfe und Frauenheilkunde 59, no. 1 (1999): 37–40. http://dx.doi.org/10.1055/s-1999-14354.

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13

Khamis, J., A. Nchimi, P. Clapuyt, and F. Bury. "RP41 Leiomyomatose œsophagienne : a propos d’un cas clinique." Journal de Radiologie 87, no. 10 (2006): 1549. http://dx.doi.org/10.1016/s0221-0363(06)87947-3.

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14

Krentel, H., and J. Hucke. "Disseminierte hormonbildende Leiomyomatose nach laparoskopischer suprazervikaler Hysterektomie: ein Fallbericht." Geburtshilfe und Frauenheilkunde 70, no. 11 (2010): 894–97. http://dx.doi.org/10.1055/s-0030-1250509.

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15

Renner, Regina, and Michael Sticherling. "Familiares Auftreten einer segmentalen Typ-2-Manifestation der kutanen Leiomyomatose. Familial occurrence of a type 2 segmental manifestation of cutaneous leiomyomatosis." Journal der Deutschen Dermatologischen Gesellschaft 3, no. 9 (2005): 695–99. http://dx.doi.org/10.1111/j.1610-0387.2005.05742.x.

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16

Junginger, Th, K. P. Maurer, V. F. Eckardt, and H. J. Rumpelt. "Sekundäre Achalasie bei niedrigmalignem Non-Hodgkin-Lymphom und Leiomyomatose der Kardia." DMW - Deutsche Medizinische Wochenschrift 117, no. 18 (2008): 698–702. http://dx.doi.org/10.1055/s-2008-1062366.

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17

Sekulic, Miroslav, Laura Moench, and Saeid Movahedi-Lankarani. "Disseminated peritoneal leiomyomatosis postmorcellated resection of uterine leiomyomatous tissue." APMIS 124, no. 12 (2016): 1063–71. http://dx.doi.org/10.1111/apm.12601.

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18

Alkatout, Ibrahim, Thilo Wedel, and Nicolai Maass. "Kombinierte Therapie der Endometriose: Radikal und schonend zugleich." Aktuelle Urologie 49, no. 01 (2018): 60–72. http://dx.doi.org/10.1055/s-0043-122175.

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ZusammenfassungEndometriose ist die zweithäufigste benigne Erkrankung des weiblichen Genitals nach der Leiomyomatose. Schwerpunkt dieser Übersicht ist die Darstellung des gynäkologischen Dilemmas zwischen medizinisch machbarem und für die individuelle Patientin sinnvollem Management. Im Vordergrund stehen die präoperative Diagnostik sowie die Planung der Operationsradikalität in Abhängigkeit des Leidensdruckes sowie des Kinderwunsches. Besonders herausgearbeitet werden die anatomischen Schnittmengenbereiche, die bei Verletzung zu (anhaltenden) Schädigungen des vorderen, mittleren und hinteren

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19

Monforte-Muñoz, Hector, Neena Kapoor, and Jorge Albores Saavedra. "Epstein-Barr Virus-associated Leiomyomatosis and Posttransplant Lymphoproliferative Disorder in a Child with Severe Combined Immunodeficiency: Case Report and Review of the Literature." Pediatric and Developmental Pathology 6, no. 5 (2003): 449–57. http://dx.doi.org/10.1007/s10024-003-8096-x.

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The occurrence of smooth muscle neoplasms and lymphoproliferative disorders in immunocompromised patients is well recognized. We report the case of an 8-year-old girl with adenosine deaminase (ADA)-deficient severe combined immunodeficiency (SCID) status post-bone marrow transplant (BMT), in whom Epstein-Barr virus (EBV) was detected in innumerable leiomyomas involving the gallbladder (leiomyomatosis), and multifocal leiomyomas in liver, spleen, pancreas, intestinal tract, and lung. The leiomyomas of the gallbladder, liver, spleen, and lung were asymptomatic, while those located in the colon b

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20

Tun, Aung Myint, Nay Min Tun, Kyaw Zin Thein, Ei Ei Naing, Shah Giashuddin, and Maxim Shulimovich. "A Rare Concurrence of Leiomyomatosis Peritonealis Disseminata, Leiomyosarcoma of the Pelvis and Leiomyomatous Nodule of the Liver." Case Reports in Oncological Medicine 2016 (2016): 1–4. http://dx.doi.org/10.1155/2016/3025432.

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Leiomyomatosis peritonealis disseminata (LPD) is a rare entity that is characterized by the presence of multiple subperitoneal or peritoneal smooth muscle nodules throughout the peritoneal surface mimicking a malignant process. LPD follows a benign course in general, and it is often found incidentally during abdominal surgery. There have been reported cases of LPD with malignant degeneration although the association is uncertain. Concurrent finding of LPD and leiomyosarcoma of the pelvis is very rare that could be coincidental, malignant transformation of LPD to leiomyosarcoma, or progression

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21

Udager, Aaron M., and Rohit Mehra. "Morphologic, Molecular, and Taxonomic Evolution of Renal Cell Carcinoma: A Conceptual Perspective With Emphasis on Updates to the 2016 World Health Organization Classification." Archives of Pathology & Laboratory Medicine 140, no. 10 (2016): 1026–37. http://dx.doi.org/10.5858/arpa.2016-0218-ra.

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Molecular and morphologic interrogation has driven a much-needed reexamination of renal cell carcinoma (RCC). Indeed, the recently released 2016 World Health Organization classification now recognizes 12 distinct RCC subtypes, as well as several other emerging/provisional RCC entities. From a clinical perspective, accurate RCC classification may have important implications for patients and their families, including prognostic risk stratification, targeted therapeutics selection, and identification for genetic testing. In this review, we provide a conceptual framework for approaching RCC diagno

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22

Wolfe, Scott, James Sullivan, and Leonard Kahn. "Perivascular Leiomyomatosis: A Unique Case Report." International Journal of Surgical Pathology 26, no. 7 (2018): 676–79. http://dx.doi.org/10.1177/1066896918772340.

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There are 3 histologically benign smooth muscle neoplasms that have unusual growth patterns. These include intravascular leiomyomatosis, benign metastasizing leiomyoma, and leiomyomatosis peritonealis desseminata. We report a unique case of perivascular leiomyomatosis. The tumor showed multiple nodules of benign smooth muscle with some of the nodules closely associated with the periphery of the medial muscle layer of venous channels. All the neoplastic nodules were located on the outer surface of venous channels, thus precluding a diagnosis of intravascular leiomyomatosis. To the best of our k

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23

Pimentel, José, Ana de Almeida, Ierecê Aymoré, Edna Pinto, Laura Osthoff, and Julius Smith. "Metastatic skeletal leiomyomatosis (leiomyomatosis ossea)." Skeletal Radiology 31, no. 1 (2001): 30–34. http://dx.doi.org/10.1007/s002560100425.

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24

Tamura, Saya, Takuma Hayashi, Hideki Tokunaga, Nobuo Yaegashi, Kaoru Abiko, and Ikuo Konishi. "Oncological Properties of Intravenous Leiomyomatosis: Involvement of Mesenchymal Tumor Stem-Like Cells." Current Issues in Molecular Biology 43, no. 2 (2021): 1188–202. http://dx.doi.org/10.3390/cimb43020084.

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Uterine leiomyoma, also known as fibroids, is the most common benign neoplasm of the female genital tract. Leiomyoma is the most common uterine tumor. The leiomyoma subtypes account for approximately 10% of leiomyomas. Intravenous leiomyomatosis, a uterine leiomyoma subtype, is an intravascular growth of benign smooth muscle cells, occasionally with pelvic or extrapelvic extension. Uterine leiomyosarcoma, a malignant tumor, tends to metastasize hematogenously, and distant metastasis to the lungs and liver is common. Therefore, the oncological properties of this intravenous leiomyomatosis resem

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25

Bristow, R. E., and F. J. Montz. "Leiomyomatosis peritonealis disseminata and ovarian Brenner tumor associated with tamoxifen use." International Journal of Gynecologic Cancer 11, no. 4 (2001): 312–15. http://dx.doi.org/10.1136/ijgc-00009577-200107000-00010.

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Abstract.Bristow RE, Montz FJ. Leiomyomatosis peritonealis disseminata and ovarian Brenner tumor associated with tamoxifen use.Tamoxifen is frequently administered as adjuvant therapy for breast carcinoma and produces weak estrogen agonist effects in estrogen sensitive tissues. In addition to producing a measurable increase in the risk of endometrial carcinoma, tamoxifen has also been associated with increasing size of uterine leiomyomata as well as the development of new leiomyomata. As the indications for tamoxifen therapy expand, surveillance for additional potential associated adverse outc

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26

Deng, Yundan, and Bing Song. "Three Case Reports of Intravenous Leiomyomatosis with Intracardiac Extensions." Thoracic and Cardiovascular Surgeon Reports 09, no. 01 (2020): e40-e43. http://dx.doi.org/10.1055/s-0040-1715183.

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Abstract Background Intravenous leiomyomatosis is a rare disease. Histologically, intravenous leiomyomatosis is a benign tumor, but its biological behavior can be malignant. The development of intracardiac extensions leads to congestive heart failure and occasionally sudden fatalities. Case Description The cases of three patients treated at our university between 2017 and 2018 were studied retrospectively. Intravenous tumors extending into the right heart system were fully removed without perioperative complications or death. Only one tumor recurrence was observed during the followed-up period

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27

TOYOTA, Kazuhiro, Katsunari MIYAMOTO, Yoshihiro SAKASHITA, et al. "A case of leiomyomatosis of the esophagus." Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association) 73, no. 4 (2012): 832–35. http://dx.doi.org/10.3919/jjsa.73.832.

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28

HIRAOKA, Kazuya, Makio NAGAOKA, Kazuo YAMABE, Shigeo FUJITA, and Toshiya MICHIURA. "A Case of Leiomyomatosis Peritonealis Disseminata." Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association) 74, no. 5 (2013): 1375–81. http://dx.doi.org/10.3919/jjsa.74.1375.

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29

Li, Rongjuan, Yanguang Shen, Yan Sun, et al. "Intravenous Leiomyomatosis with Intracardiac Extension: Echocardiographic Study and Literature Review." Texas Heart Institute Journal 41, no. 5 (2014): 502–6. http://dx.doi.org/10.14503/thij-13-3533.

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Uterine leiomyomatosis is a common disease in women; however, intravenous leiomyomatosis with intracaval and intracardiac tumor extension is rare. We sought to analyze the clinical and echocardiographic features of intracardiac leiomyomatosis. From January 2003 through July 2012, 7 women (age range, 24–59 yr) underwent surgical resection of histopathologically diagnosed intracardiac leiomyomas at our hospital. Most of the patients had histories of hysterectomy or uterine leiomyoma. We retrospectively analyzed their preoperative echocardiograms. We found that the tumors had no stalks, did not a

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30

Konrad, Peter, and Lennart Mellblorn. "Intravenous Leiomyomatosis." Acta Obstetricia et Gynecologica Scandinavica 68, no. 4 (1989): 371–76. http://dx.doi.org/10.3109/00016348909028675.

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31

John, DeepakGeorge, Krishna Muralitharan, KS Saravana Krushna Raja, and N. Sritharan. "Intravenous leiomyomatosis." Indian Journal of Vascular and Endovascular Surgery 7, no. 3 (2020): 294. http://dx.doi.org/10.4103/ijves.ijves_94_19.

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32

Sinha, Rakesh, Meenakshi Sundaram, and Smita Lakhotia. "Recurrent Leiomyomatosis." Journal of Minimally Invasive Gynecology 16, no. 6 (2009): 667–68. http://dx.doi.org/10.1016/j.jmig.2009.02.006.

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33

Sandoval-Herrera, C., A. Gupta, and K. Litvinova. "Parasitic Leiomyomatosis." Journal of Minimally Invasive Gynecology 27, no. 7 (2020): S144. http://dx.doi.org/10.1016/j.jmig.2020.08.282.

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34

Kullo, Iftikhar J., Jae K. Oh, Gary L. Keeney, Bijoy K. Khandheria, and James B. Seward. "Intracardiac Leiomyomatosis." Chest 115, no. 2 (1999): 587–91. http://dx.doi.org/10.1378/chest.115.2.587.

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35

Parikh, J., and A. Lesseps. "Intravenous leiomyomatosis." Journal of Obstetrics & Gynaecology 20, no. 4 (2000): 439–40. http://dx.doi.org/10.1080/01443610050112264.

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36

Levine, M. S., J. L. Buck, L. Pantongrag-Brown, P. C. Buetow, M. A. Lowry, and L. H. Sobin. "Esophageal leiomyomatosis." Radiology 199, no. 2 (1996): 533–36. http://dx.doi.org/10.1148/radiology.199.2.8668807.

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37

Andreeva, Yu Yu, G. A. Frank, A. A. Shikeeva, et al. "Intravascular leiomyomatosis." Arkhiv patologii 77, no. 3 (2015): 51. http://dx.doi.org/10.17116/patol201577351-56.

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38

Urkmez, Asli, Ilgen Ertam, Isil Kilinc Karaarslan, Alican Kazandi, and Can Ceylan. "Leiomyomatosis Cutis." Turkish Journal of Dermatology / Türk Dermatoloji Dergisi 5, no. 4 (2011): 101–3. http://dx.doi.org/10.5152/tdd.2011.22.

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39

Hayasaka, Kazumasa, Yoshiaki Tanaka, Motoaki Fujii, Kazuhisa Himi, and Nanao Negishi. "Intravenous Leiomyomatosis." Journal of Computer Assisted Tomography 24, no. 1 (2000): 83–85. http://dx.doi.org/10.1097/00004728-200001000-00017.

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40

Bewersdorf, Tim, and Alexander Loch. "Intracardiac leiomyomatosis." European Heart Journal 39, no. 41 (2018): 3750. http://dx.doi.org/10.1093/eurheartj/ehy415.

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41

Lo, K. W. K., and T. K. Lau. "Intracardiac leiomyomatosis." Archives of Gynecology and Obstetrics 264, no. 4 (2001): 209–10. http://dx.doi.org/10.1007/s004040000115.

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42

Rausch, S., M. Scharpf, H. Moch, A. Stenzl, and J. Bedke. "Leiomyomatöses Nierenzellkarzinom." Der Urologe 55, no. 3 (2015): 376–80. http://dx.doi.org/10.1007/s00120-015-3975-0.

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43

Diakomanolis, E., A. Elsheikh, M. Sotiropoulou, et al. "Intravenous leiomyomatosis." Archives of Gynecology and Obstetrics 267, no. 4 (2003): 256–57. http://dx.doi.org/10.1007/s00404-002-0443-z.

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44

Grella, Louis, Thomas E. Arnold, Kara H. V. Kvilekval, and Fabio Giron. "Intravenous leiomyomatosis." Journal of Vascular Surgery 20, no. 6 (1994): 987–94. http://dx.doi.org/10.1016/0741-5214(94)90237-2.

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45

Li, Qiang, Jie Ma, Bin Hao, Xintao Pi, and Hao Li. "One-Stage Surgical Removal of Intravenous Leiomyomatosis with Right Heart Extension is Safe." Heart Surgery Forum 14, no. 3 (2011): 192. http://dx.doi.org/10.1532/hsf98.20101150.

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Intravenous leiomyomatosis is a rare smooth muscle tumor. We report the case of a 42-year-old woman with both intravenous and intracardiac extension of leiomyomatosis who underwent 3 operations within 9 years. During the last admission, she underwent a successful single-stage surgical approach while under cardiopulmonary bypass with circulatory arrest. A postoperative histopathologic examination of the resected specimen confirmed the diagnosis.

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46

Goldsmith, P., J. V. Soames, and D. Meikle. "Leiomyomatous hamartoma of the posterior tongue: a case report." Journal of Laryngology & Otology 109, no. 12 (1995): 1190–91. http://dx.doi.org/10.1017/s0022215100132402.

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AbstractA case of a rare leiomyomatous hamartoma arising in the posterior tongue of a sixteen-month-old male is reported. There has been no recurrence following simple excision and presenting symptoms of choking on swallowing have resolved. Most other leiomyomatous hamartomas in the upper aerodigestive tract have been reported in Japanese patients and have involved the maxillary gingiva and hard palate.

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47

Khalid, Nazish, Faizan Ullah, Jhanzeb Iftikhar, Taskheer Abbas, Osama Shakeel, and Aamir Syed. "Disseminated Peritoneal Leiomyomatosis: A Case Report." International Journal of Medical Reviews and Case Reports 4, Reports in Surgery, Urology and (2020): 73. http://dx.doi.org/10.5455/ijmrcr.disseminated-peritoneal-leiomyomatosis.

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48

Lamba, Manisha, Shailendra Verma, Robert Prokopetz, Tadeusz A. Pierscianowski, Maha Jabi, and Terence Moyana. "Multiple Cutaneous and Uterine Leiomyomas Associated with Gastric Gist." Journal of Cutaneous Medicine and Surgery 9, no. 6 (2005): 332–35. http://dx.doi.org/10.1177/120347540500900609.

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Background: There are a number of reports documenting familial cases of leiomyomatosis cutis associated with uterine leiomyomata. However, to our knowledge, the association of gastrointestinal stromal tumour (GIST) with this entity has not as yet been reported. We report an interesting case of cutaneous leiomyomatosis, metachronous uterine leiomyomata, and a gastric GIST in a 43-year-old woman. Observation: The patient had previously undergone two separate uterine myomectomies at ages 25 and 26 years, respectively, followed by a hysterectomy at 27 years. At 36 years she underwent partial gastr

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49

Zaporozhchenko, M. B., D. Y. Parubina, and A. V. Sidorenko. "Infectious aspects of tissues of leiomyomatous nodules removed in women of reproductive age, patients with uterine leiomyoma." Reports of Vinnytsia National Medical University 22, no. 1 (2018): 24–28. http://dx.doi.org/10.31393/reports-vnmedical-2018-22(1)-05.

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The state of the microbial ecology of genital organs in women of reproductive age deserves special attention of the doctor-clinician. Infections of the genital tract are recognized as one of the triggers of uterine myoma. Leiomyoma of the uterus can arise as a result of lesions of the myometrium by inflammatory processes. The goal is to examine the tissues of distant leiomyomatous nodules for the presence of an associated microbial flora in women of reproductive age who suffer from asymptomatic and symptomatic clinical course of the uterine leiomyoma. The presence of infectious flora in the va

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50

Azzie, G., A. Bensoussan, and L. Spitz. "The association of anorectal leiomyomatosis and diffuse oesophageal leiomyomatosis." Pediatric Surgery International 19, no. 6 (2003): 424–26. http://dx.doi.org/10.1007/s00383-003-0955-z.

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