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Lymphangioma

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https://www.readbyqxmd.com/read/29151529/rare-case-of-pancreatic-cystic-lymphangioma
#1
Masakuni Fujii, Hiroaki Saito, Masao Yoshioka, Junji Shiode
Pancreatic cystic lymphangioma is an extremely rare tumor. The characteristic imaging findings are poorly defined, and distinguishing between this disease and other pancreatic cyst-related tumors is very difficult. We herein report a case of a Japanese woman in her 50s with this lesion, located in the tail of the pancreas. Pancreatic cystic lymphangioma should therefore be considered in the differential diagnosis of pancreatic cystic lesions. Laparoscopic resection can be a useful, minimally invasive surgical approach for treating these cysts as well as for the treatment of benign or low-grade malignant tumors located in the pancreatic body or tail...
November 20, 2017: Internal Medicine
https://www.readbyqxmd.com/read/29138659/-lymphangioma-of-the-breast-about-a-case
#2
Eric Mbuya Musapudi, Aimé Lukoba Bwalya, Igor Mujinga Wa Mujinga, Didier Tshibangu Mujinga, Julien Ilunga Nikulu, Guy Nday Ilunga
Lymphangioma is a benign lesion of the lymphatic vessels. It is a rare paediatric condition and it is exceptional among adults. It mainly occurs in the neck, armpit and abdomen. It rarely occurs in the breast. We report the case of a 18 year-old female patient seen in consultation for a mass in her left breast, which had evolved over the last 23 months. Management was based on surgery. The patient underwent complete tumor resection. Anatomopathological examination showed lymphangioma of the breast. Patient's evolution was favorable and the patient had a median 10 months follow-up with no recurrences identified...
2017: Pan African Medical Journal
https://www.readbyqxmd.com/read/29119576/natural-course-of-fetal-axillary-lymphangioma-based-on-prenatal-ultrasound-studies
#3
Theera Tongsong, Suchaya Luewan, Jiraporn Khorana, Sirinart Sirilert, Cholaros Charoenratana
This series and literature review aimed to prenatally characterize the nature of axillary lymphangioma. A total of 30 cases, including our 5 cases, were analyzed. Insights gained from this review are as follows: Septate and nonseptate cysts seem to be different entities. The nonseptate type tends to be small and transient but more highly associated with aneuploidies. Septate cysts are very rarely associated with other abnormalities and hydrops fetalis, unlike cystic hygroma colli, but are more progressive with gestational age and associated with adverse outcomes...
November 9, 2017: Journal of Ultrasound in Medicine: Official Journal of the American Institute of Ultrasound in Medicine
https://www.readbyqxmd.com/read/29114705/splenic-lymphangioma-in-an-adult
#4
Safa A Al-Shaikh, Aalaa M Mubarak, Zainab F Harb
Splenic lymphangiomas are exceedingly rare benign neoplasms that occur mainly in children. They are commonly seen in the neck and axillary region. Abdominal lymphangiomas accounts for less than 5% of cases. So far, fewer than 100 cases of spleen lymphangiomas have been reported in the literature. In this paper, we present one case of solitary splenic lymphangioma in a 34-year-old woman who presented with abdominal pain and weight loss for one month. The patient underwent splenectomy and diagnosis was confirmed by histopathology and immunohistochemistry studies...
November 2017: Saudi Medical Journal
https://www.readbyqxmd.com/read/29113789/a-case-of-lymphangioma-like-mesenteric-cysts-diagnosed-as-adenocarcinoma-of-possible-pancreatic-origin-on-eus-fna
#5
Maxime Delvincourt, Edmund M Godfrey, Adam Duckworth, Nicholas R Carroll
No abstract text is available yet for this article.
November 4, 2017: Gastrointestinal Endoscopy
https://www.readbyqxmd.com/read/29081933/cystic-intra-abdominal-masses-in-children
#6
Luisa Ferrero, Riccardo Guanà, Giulia Carbonaro, Maria Grazia Cortese, Luca Lonati, Elisabetta Teruzzi, Jurgen Schleef
Benign intra-abdominal cystic masses in infancy are fairly uncommon and their etiopathogenesis, histology and clinical presentation differ significantly. Our aim is to report our experience in their treatment in order to discuss the best diagnostic and treatment modality. The medical records of 5 children (2M, 3F) with cystic intraabdominal masses referred to our hospital between November 2012 and September 2016, were retrospectively reviewed. All patients underwent open surgery and subsequent histopathologic analysis...
October 6, 2017: Pediatric Reports
https://www.readbyqxmd.com/read/29077628/vulvar-lymphangioma-circumscriptum-treated-with-fractional-ablative-erbium-yttrium-aluminium-garnet-laser
#7
Joy Makdisi, Sebastien de Feraudy, Christopher B Zachary
No abstract text is available yet for this article.
October 26, 2017: Dermatologic Surgery: Official Publication for American Society for Dermatologic Surgery [et Al.]
https://www.readbyqxmd.com/read/29077499/human-immunodeficiency-virus-negative-associated-lymphangioma-like-kaposi-s-sarcoma-with-variable-clinical-presentationsa-case-report
#8
Georgios Kotzias, Modupe Agunbiade, Leon Isaac, Morteza Khaladj
Lymphangioma-like Kaposi's sarcoma (LLKS) is a rare histologic variant of KS. Kaposi's sarcoma is also known as human herpesvirus type 8. The clinical presentation of the LLKS lesion is highly unusual and similar to that of classic KS but with multinodular vascular tumors and lymphedema. We present a 63-year-old native Haitian man with multiple slowly progressive exophytic ulcerated lesions covering more than 60% of his left lower extremity with no systemic involvement. Much confusion surrounded the clinical presentation of these wounds, and we postulated several differential diagnoses...
September 2017: Journal of the American Podiatric Medical Association
https://www.readbyqxmd.com/read/29062665/spontaneous-regression-of-lymphangiomas-in-a-single-center-over-34-years
#9
Motoi Kato, Shoji Watanabe, Reiko Kato, Hiroshi Kawashima, Takuya Iida, Azusa Watanabe
BACKGROUND: A lymphangioma, also called a lymphatic malformation, is a congenital condition that frequently occurs in young children. It is classified into 3 groups depending on the size of the cysts (macrocystic, microcystic, and mixed). Spontaneous regression occurs in some cases; however, the characteristics of patients who show regression have not been studied previously. Furthermore, the types and the timing of the initial treatment are still controversial. Therefore, we statistically analyzed the occurrence of short-term spontaneous regression, patient age at original occurrence, cyst types, cyst sizes, and cyst locations in patients diagnosed with peripheral localized lymphangiomas in a single children center over 34 years...
September 2017: Plastic and Reconstructive Surgery. Global Open
https://www.readbyqxmd.com/read/29061139/evaluation-of-lymphatic-vessel-dilatations-by-anterior-segment-swept-source-optical-coherence-tomography-case-report
#10
Eva Volek, Jeannette Toth, Zoltan Zsolt Nagy, Miklos Schneider
BACKGROUND: Conjunctival lymphangiectasia is a rare condition presumably caused by the obstruction of lymphatic channels or by an abnormal connection between conjunctival lymphatic and blood vessels. Diagnosis is based on clinical appearance and histology. We report a case of conjunctival lymphangiectasia in which anterior segment optical coherence tomography (OCT) was used to assist the diagnosis and the planning of the biopsy location. CASE PRESENTATION: A 31-year-old woman was referred with repeated episodes of conjunctival "hemorrhages" and chemosis with extended recovery periods over the last months...
October 23, 2017: BMC Ophthalmology
https://www.readbyqxmd.com/read/29046074/large-cystic-lympangioma-of-the-pancreas-a-case-reportum
#11
S N Jayappa, P Rao, A S Tandon, Kgs Bharathy, S S Sikora
Lymphangioma of the pancreas is rare and presents as a large cystic mass in the retroperitoneum. The pancreatic origin can be confirmed by careful evaluation of cross sectional imaging. Preoperative differentiation from other pancreatic cystic neoplasms is difficult but possible. Large symptomatic lesions warrant surgery. The diagnosis is confirmed by typical features on histopathology and immunohistochemistry. Presented here is a case report of a pancreatic lymphangioma, discussed in the context of available literature...
October 19, 2017: Annals of the Royal College of Surgeons of England
https://www.readbyqxmd.com/read/28988459/inconsistency-in-classifying-vascular-anomalies-what-s-in-a-name
#12
Kristy S Pahl, Kyung Kim, Casey Sams, Hortensia Alvarez, Scott V Smith, Julie Blatt
BACKGROUND: Vascular anomalies are a heterogeneous group of disorders seen in children and adults. A standard nomenclature for classification has been offered by the International Society for the Study of Vascular Anomalies. Its application is important for communication among the multiple specialties involved in the care of patients and for planning treatment, as well as for research and billing. We hypothesized that terminology still is not uniformly applied, and that this could have an impact on treatment...
October 8, 2017: Pediatric Blood & Cancer
https://www.readbyqxmd.com/read/28976139/cystic-lymphangioma-of-the-lesser-omentum-in-a-pregnant-woman-a-case-report-and-review-of-the-literature
#13
Ozhan Ozdemir, Mustafa Erkan Sarı, Cemal Resat Atalay, Yüksel Kurban, Vusale Asgarova, Devrim Tuba Unal
Lymphangiomas are rare benign tumors which are generally seen in pediatric population and the etiopathogenesis has not yet been understood. They occasionally occur in the head and neck or axillary region with only 5% of them being located in the abdominal or mediastinal cavity. These tumors may be asymptomatic or may cause acute abdominal symptoms due to the location and extention. In the English literature, only 4 cases of lymphangioma were reported to have occurred in the pregnancy period. Herein, we report a case of cystic lymphangioma of the lesser omentum detected incidentally on the ultrasonogram of a 21 year-old, 26-week pregnant woman...
September 2017: Journal of Experimental Therapeutics & Oncology
https://www.readbyqxmd.com/read/28958247/cystic-lymphangioma-of-the-mesenteric-root-in-an-adolescent-an-operative-challenge
#14
Colin Muncie, Michael Morris, Christopher Blewett
No abstract text is available yet for this article.
September 1, 2017: American Surgeon
https://www.readbyqxmd.com/read/28955596/cavernous-lymphangioma-of-the-tongue-in-an-adult-a-case-report
#15
Selin Eren, Ahmet Taylan Cebi, Sabri Cemil Isler, Metin Berk Kasapoglu, Nihan Aksakalli, Cetin Kasapoglu
Lymphangioma is a benign hamartomatous lesion caused by congenital malformation of the lymphatic system. This benign tumor is detected most commonly at birth or in early childhood but rarely in adults. On clinical examination, most lymphangiomas contain clear lymph fluid, but some may present as transparent vesicles containing red blood cells due to hemorrhage. In addition, lymphangioma may occur in association with hemangioma. This tumor occurs most commonly in the head and neck area, but rarely in the oral cavity...
2017: J Istanb Univ Fac Dent
https://www.readbyqxmd.com/read/28940760/acquired-progressive-lymphangioma-case-report-with-partial-response-to-imiquimod-5-cream
#16
Andac Salman, Gonca Sarac, Burce Can Kuru, Leyla Cinel, Ayse Deniz Yucelten, Tulin Ergun
Acquired progressive lymphangioma (APL), or benign lymphangioendothelioma, is an unusual entity derived from vascular structures. Clinically and histopathologically it may resemble Kaposi's sarcoma and well-differentiated angiosarcoma, causing a diagnostic problem. We report an individual with APL initially diagnosed with Kaposi's sarcoma who underwent unnecessary laboratory testing. Imiquimod 5% cream stopped the progression of the lesion. Awareness of this rare entity may prevent patients from undergoing excessive testing...
September 21, 2017: Pediatric Dermatology
https://www.readbyqxmd.com/read/28932041/hemangiolymphangioma-of-buccal-mucosa-a-rare-case-report
#17
Selvamani Manickam, Prem Sasikumar, B Nanda Kishore, Sheethal Joy
Vascular anomalies are mainly classified under two headings, i.e. under vascular tumors and vascular malformations. Hemangioma and lymphangioma are examples for such a vascular anomalies. Malformations may be seen in different combinations of vascular elements, and histologically these vessels may be filled with blood and named lymphangiohemangioma or hemangiolymphangioma according to the dominant tissue structure present. It is a rare developmental anomaly. This paper reports a case of lymphangiohemangioma in a 21-year-old female patient...
May 2017: Journal of Oral and Maxillofacial Pathology: JOMFP
https://www.readbyqxmd.com/read/28927352/an-acute-presentation-of-pediatric-mesenteric-lymphangioma-a-case-report-and-literature-overview
#18
Céline Clement, Rob Snoekx, Pieter Ceulemans, Inez Wyn, Jan Matheï
INTRODUCTION: Lymphangioma accounts for 5% of benign pediatric tumors and less than 1% is located in the abdomen. While mesenteric lymphatic malformation or mesenteric lymphangioma (ML), mostly appears asymptomatic in adults, an acute clinical presentation is seen more often in children. Symptoms can mimic obstruction or peritonitis and diagnosis can therefore be challenging. Imaging studies are performed to exclude other causes of obstruction or peritonitis. Diagnosis of ML is always made by histology...
September 19, 2017: Acta Chirurgica Belgica
https://www.readbyqxmd.com/read/28913305/treatment-of-tongue-lymphangioma-with-intralesional-combination-injection-of-steroid-bleomycin-and-bevacizumab
#19
Jungil Hwang, Yung Ki Lee, Jin Sik Burm
Lymphangioma is a congenital malformed lymphatic tumor that rarely involves the tongue. In our clinic, a 10-year-old female presented with lymphangioma circumscriptum involving the right two-thirds of the tongue. We administered an intralesional combination injection of triamcinolone, bleomycin, and bevacizumab as a treatment. Almost complete remission after combination therapy was achieved without complications such as edema, swallowing difficulties or recurrence. Bevacizumab, an inhibitor of vascular endothelial growth factor, was effective for the treatment of lymphangioma of the tongue in this case...
March 2017: Arch Craniofac Surg
https://www.readbyqxmd.com/read/28905842/malignant-perivascular-epithelioid-cell-tumor-of-the-orbit-report-of-a-case-and-review-of-literature
#20
Md Shahid Alam, Bipasha Mukherjee, S Krishnakumar, Jyotirmay Biswas
Perivascular epithelioid cell tumor (PEComa) is a rare neoplasm considered to arise from myomelanocytic cell lineage. The uterus is reportedly the most common site to be involved. Orbital PEComa is extremely rare with only two cases reported till date. A 5-year-old male presented with a right medial orbital mass for the last 6 months. The patient was diagnosed with alveolar soft part sarcoma elsewhere. Magnetic resonance imaging features were suggestive of lymphangioma with bleeding. The excision biopsy revealed multiple tumor cells comprising epithelioid cells with clear cytoplasm, along with nuclear atypia and mitosis...
September 2017: Indian Journal of Ophthalmology
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