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Smooth Muscle Hamartoma

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1. Congenital Linear Smooth Muscle Hamartoma with Hypertrichosis: Hair Density on Dermoscopy in Parallel with the Number of Smooth Muscle Bundles (PubMed)

Congenital Linear Smooth Muscle Hamartoma with Hypertrichosis: Hair Density on Dermoscopy in Parallel with the Number of Smooth Muscle Bundles 29386851 2018 11 13 1013-9087 30 1 2018 Feb Annals of dermatology Ann Dermatol Congenital Linear Smooth Muscle Hamartoma with Hypertrichosis: Hair Density on Dermoscopy in Parallel with the Number of Smooth Muscle Bundles. 114-116 10.5021/ad.2018.30.1.114 Son Jin-Hwa JH Department of Dermatology, Pusan National University School of Medicine, Busan, Korea

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2017 Annals of dermatology

2. Smooth Muscle Hamartoma

Smooth Muscle Hamartoma Smooth Muscle Hamartoma Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Smooth Muscle Hamartoma Smooth Muscle (...) Hamartoma Aka: Smooth Muscle Hamartoma II. Signs and Overlies a firm nodular base Lesion may "ripple" when stroked III. Distribution Anywhere IV. Differential Diagnosis Congenital Malanocytic (distinguish with biopsy) V. Labs Biopsy shows s VI. Course No increased risk of malignant transformation VII. Management None Images: Related links to external sites (from Bing) These images are a random sampling from a Bing search on the term "Smooth Muscle Hamartoma." Click on the image (or right click) to open

2018 FP Notebook

3. A rare pulmonary hamartoma: fibroleiomyomatous hamartoma (PubMed)

A rare pulmonary hamartoma: fibroleiomyomatous hamartoma Pulmonary hamartomas are more common than expected because they are usually asymptomatic and are either discovered on routine chest radiography or when they are noted incidentally in approximately 0.25 % of autopsies. In contrast, pulmonary fibroleiomyomatous hamartoma, which consists of interlacing bundles of smooth muscle cells admixed with fibrous tissue and numerous tubular or cleft-like epithelial inclusions, is a rare type (...) of hamartoma. Controversy exists regarding the pathogenesis of this tumor. We herein present a rare case of a 68-year-old male patient without a pre-existing smooth muscle tumor, who underwent resection for a tumor that was considered to be a true pulmonary fibroleiomyomatous hamartoma.

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2016 Surgical Case Reports

4. Cystic lung lesions mimicking hydatidosis: hamartoma or benign metastazing leiomyoma? (PubMed)

Cystic lung lesions mimicking hydatidosis: hamartoma or benign metastazing leiomyoma? We report an unusual case of a 53-year-old woman who presented with multiple lung cystic lesions presumed to be related to pulmonary hydatidosis, treated and followed for 3 years before surgical removal was decided. Unexpectedly, pathological findings showed the presence of benign spindle cell proliferation. Immunohistochemical staining confirmed the smooth muscle nature of the spindle cells which were also

2019 Annals of Thoracic Surgery

5. A congenital smooth muscle hamartoma masquerading as a reticulate vascular naevus. (PubMed)

A congenital smooth muscle hamartoma masquerading as a reticulate vascular naevus. Smooth muscle hamartoma (SMH) is a benign congenital or acquired hamartomatous lesion comprising a dermal proliferation of smooth muscle bundles. We report a case of congenital SMH with an unusual clinical appearance. A 3-year-old girl presented with an asymptomatic atrophic linear lesion on the posterior surface of her right thigh, which had been present since birth. The striking resemblance to a vascular lesion

2013 Clinical & Experimental Dermatology

6. Lingual Leiomyomatous Hamartoma in an Adult Male (PubMed)

Lingual Leiomyomatous Hamartoma in an Adult Male An otherwise healthy 20-year-old male presented with an exophytic, polypoid, yellowish lesion involving the dorsal surface of his tongue, which he reported being present since birth and unchanged. This was removed by surgical excision and diagnosed as a leiomyomatous hamartoma. Histological examination revealed a combination of fibrovascular connective tissue, conspicuous smooth-muscle bundles, adipose tissue, minor salivary gland tissue, blood (...) vessels, lymphoid tissue, peripheral nerves, and normal skeletal muscle. This case is exceptional due to the patient's age, as until now, lingual leiomyomatous hamartomas have been reported almost exclusively in a paediatric population. To our knowledge, this is the eldest age at which a LLH has been reported in the literature. This underscores the need for clinicians to consider this rarely reported entity when considering the radiographic and clinical differential diagnoses for these lesions, both

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2018 Case reports in dentistry

7. Smooth Muscle Hamartoma

Smooth Muscle Hamartoma Smooth Muscle Hamartoma Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Smooth Muscle Hamartoma Smooth Muscle (...) Hamartoma Aka: Smooth Muscle Hamartoma II. Signs and Overlies a firm nodular base Lesion may "ripple" when stroked III. Distribution Anywhere IV. Differential Diagnosis Congenital Malanocytic (distinguish with biopsy) V. Labs Biopsy shows s VI. Course No increased risk of malignant transformation VII. Management None Images: Related links to external sites (from Bing) These images are a random sampling from a Bing search on the term "Smooth Muscle Hamartoma." Click on the image (or right click) to open

2015 FP Notebook

8. Hamartomas from head to toe: an imaging overview (PubMed)

Hamartomas from head to toe: an imaging overview Hamartomas are tumours composed of mesenchymal tissues such as cartilage, fat, connective tissue and smooth muscle and can be found in virtually any organ system. These masses commonly develop sporadically, but are also seen in certain syndromes such as tuberous sclerosis or Carney triad. While their imaging appearance varies depending on the organ they arise from, findings are usually unique and a diagnosis can be confidently made. Radiologists

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2017 The British journal of radiology

9. Reconstruction Approach to a Rare Case of Acquired Scrotal Giant Muscular Hamartoma (PubMed)

Reconstruction Approach to a Rare Case of Acquired Scrotal Giant Muscular Hamartoma Acquired scrotal giant muscular hamartoma is an uncommon benign lesion with fewer than 10 documented cases all over the world. It is characterized by a proliferation of dermal smooth muscle bundles of scrotum dartos fascia. The authors report a rare case of acquired scrotal giant muscular hamartoma, which occurred in a 70-year-old severely obese and diabetic man presenting with a progressive scrotal enlargement (...) and swelling in the last year, causing marked reduction in quality of life and cosmetic problems. The patient underwent a wide excision of the hamartomatous lesion, and then, a reductive scrotoplasty and autologous skin grafting of penis were performed. Anatomopathological examination showed an acquired scrotal giant muscular hamartoma arising from muscular fascia of dartos. This surgical technique is a valid, safe, effective, and minimally invasive option to treat this pathology, achieving both excellent

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2016 Plastic and Reconstructive Surgery Global Open

10. Intramural chondroid hamartoma in the distal esophagus in an adult: A case report and review of the literature (PubMed)

Intramural chondroid hamartoma in the distal esophagus in an adult: A case report and review of the literature Hamartoma of the esophagus is a rare lesion and the number of cases reported in the literature to date is limited. The majority of hamartomas are intraluminal tumors located in the upper third of the esophagus. Histopathologically, the majority of these tumors comprise a mixture of adipose tissue, skeletal/smooth muscle tissue, vascular components and fibrous connective tissue. We (...) herein present the case of a 33-year-old man with an intramural chondroid hamartoma located in the lower third of the esophagus. The patient underwent esophagotomy and the histopathological examination revealed that the tumor was mainly composed of chondroid tissue (60%) admixed with adipose tissue (25%) and fibrous connective tissue (15%). The aim of this study was to describe another variant of esophageal hamartoma, which exhibits a versatile phenotype.

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2016 Molecular and clinical oncology

11. Robotic-assisted laparoscopic partial cystectomy for symptomatic urachal hamartoma (PubMed)

Robotic-assisted laparoscopic partial cystectomy for symptomatic urachal hamartoma We report a case of an urachal hamartoma in a 30-year-old African American woman. The urachal lesion was excised with a robotic-assisted laparoscopic partial cystectomy. Pathologic analysis revealed cysts, smooth muscle, and ciliated epithelium consistent with a hamartoma. The patient recovered without complication. This case highlights an unusual pathology that is infrequently reported following urachal remnant

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2016 Turkish journal of urology

12. Fibrous hamartoma of infancy: a clinicopathologic analysis of 60 cases. (PubMed)

triphasic elements of mature fibrous tissue, mature adipose tissue, and immature mesenchymal tissue in varying proportions, with the additional pseudoangiomatous pattern in 32 cases. Immunohistochemical analysis demonstrated reactivity for smooth muscle actin and CD34 in the mature fibrous tissue, S100 protein in the mature adipose tissue, and variable CD34 reactivity in immature mesenchymal and pseudoangiomatous foci. Ki-67 proliferative activity was noted in the immature mesenchymal (...) Fibrous hamartoma of infancy: a clinicopathologic analysis of 60 cases. Fibrous hamartoma of infancy is a benign soft tissue tumor with a characteristic triphasic organoid histologic appearance. It typically occurs within the first 2 years of life. The usual anatomic locations include the upper extremities, axilla, and upper back. Diagnostic challenges occur when this tumor arises in older children, outside of the usual anatomic sites, or when unusual histologic features are encountered

2014 American Journal of Surgical Pathology

13. Hamartoma, Lung

; but subsequently, nonfunctioning extra-adrenal paragangliomas were added, such as gastric gastrointestinal stromal tumors (GISTs) and pulmonary chondromas. In most patients, only 2 of the 3 tumors are present at the time of diagnosis. Typically, the triad affects young people. The triad is not to be confused with the related Carney-Stratakis syndrome or the unrelated Carney complex. [ , , , ] A partial Carney triad may be seen when pulmonary hamartomas coexist with smooth muscle tumors of the stomach (...) , and dyspnea. Complications such as postobstructive pneumonia and lobar atelectasis may occur. Hemoptysis can occur if it impinges on vascular structures and causes invasion or perforation. [ ] PH usually presents with a round shape and smooth margins. The main CT features are intranodular fat and popcorn-like calcifications. [ ] (Evidence of a pulmonary hamartoma is seen in the image below.) Posteroanterior (PA) chest radiograph in a man shows an incidental coin lesion in the right midzone

2014 eMedicine Radiology

14. Rare Benign Entities of the Breast – Myoid Hamartoma and Capillary Hemangioma (PubMed)

Rare Benign Entities of the Breast – Myoid Hamartoma and Capillary Hemangioma Hamartomas can occur in different areas of the breast, but they are rarely found in the breast. Myoid hamartomas with smooth muscle cells of the type described here are particularly unusual. The pathogenesis of this benign entity with its tendency to growth and recurrence is not clear. Excision is the therapy of choice. Capillary hemangiomas are rare vascular malformations of the breast which, in contrast (...) to cavernous hemangiomas, usually remain clinically occult. It is important to differentiate these benign findings from malignant angiosarcoma. The possible heterogeneities between myoid hamartoma and capillary hemangioma using current breast imaging methods for the differential diagnosis (high-resolution ultrasound, duplex sonography, shear wave elastography, digital mammography, minimally invasive intervention) are discussed together with an overview of the literature.

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2012 Geburtshilfe Und Frauenheilkunde

15. Leiomyomatous hamartoma of the midline maxillary gingival presenting as a congenital epulis: a case report with an immunohistochemical study. (PubMed)

Leiomyomatous hamartoma of the midline maxillary gingival presenting as a congenital epulis: a case report with an immunohistochemical study. An otherwise-healthy 2-year-old Japanese female presented with a polyp-like lesion on the palatal surface at the incisive papilla. The appearance of the lesion was similar to that of a congenital epulis. The histological findings showed proliferating mesenchymal components that contained mainly smooth muscle admixed with collagen fibres, nerve fibres (...) , small vessels and mucous salivary glands. The immunohistochemical staining findings for α-smooth-muscle actin, desmin and S-100 protein were all positive. The histological diagnosis was therefore leiomyomatous hamartoma, based on clinical microscopic observations.Copyright © 2011 International Association of Oral and Maxillofacial Surgeons. Published by Elsevier Ltd. All rights reserved.

2011 International Journal of Oral and Maxillofacial Surgery

16. Hamartoma of the thoracic wall (PubMed)

Hamartoma of the thoracic wall 5075624 1972 11 29 2018 11 13 0040-6376 27 4 1972 Jul Thorax Thorax Hamartoma of the thoracic wall. 500-2 Gupta S S Pal N C NC eng Journal Article England Thorax 0417353 0040-6376 IM Adipose Tissue pathology Adolescent Bone and Bones pathology Hamartoma pathology surgery Hemangioma, Cavernous pathology Humans Lymphoid Tissue pathology Male Muscle, Smooth pathology Nerve Tissue pathology Ribs pathology Thoracic Neoplasms pathology surgery Thoracic Vertebrae

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1972 Thorax

17. Myoid (Muscular) Hamartoma of the Breast: Case Report and Review of the Literature (PubMed)

Myoid (Muscular) Hamartoma of the Breast: Case Report and Review of the Literature BACKGROUND: Myoid (muscular) hamartoma (MH) of the breast is a rare benign tumour-forming lesion composed of differentiated mammary glandular and stromal structures, fatty tissue, and areas of smooth muscle. It is considered to be a variant of mammary hamartoma. CASE REPORT: We report the case of a 46-year-old woman with MH, and provide a literature review explaining the origin of smooth muscle cells (...) . Histologically, the tumour consisted of fibrolipomatous stroma containing ductal and lobular structures of the mammary gland located mainly at the tumour borders. The glandular structures showed signs of micro- and macrocystic changes, apocrine metaplasia, and adenosis. The dominant feature was the presence of a fascicular formation of spindle cells, predominantly in central parts, with incursion between glandular structures. Immunohistochemically, foci of smooth muscle tissue were positive for desmin

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2010 Breast Care

18. A case of diffuse pilar leiomyoma or acquired smooth muscle hamartoma? (PubMed)

A case of diffuse pilar leiomyoma or acquired smooth muscle hamartoma? A 62-year-old woman presented with a skin-coloured indurated asymptomatic plaque, 150 mm in diameter on the knee. Histological analysis of a skin biopsy taken from the lesion showed haphazardly arranged bundles of smooth muscle in the deep dermis, characteristic of a pilar leiomyoma. Cutaneous pilar leiomyomas are rare, benign smooth muscle tumours arising from the arrector pili muscle, which usually appear as red or brown (...) papules < 15 mm in diameter. This case is unusual in its clinical appearance and size, being at least 10 times larger than the largest previously documented cutaneous pilar leiomyoma. Similar lesions have also been previously reported under the term 'acquired smooth muscle hamartoma' (ASMH). These cases are also rare and have no known consistent clinical features. Histologically it is difficult to differentiate between ASMH and leiomyomas, and some authors would consider this case as a new report

2009 Clinical & Experimental Dermatology

19. Risk Factors for Endometrial Cancer - A review of the evidence

International Agency for Research on Cancer (2015): Categories of evidence of carcinogenicity 88 Table C.2 World Cancer Research Fund/American Institute for Cancer Research (2018): Criteria for grading evidence for cancer prevention 90 Endometrial cancer risk factors: a review of the evidence 6 Introduction 1 1.1 Context There are two major types of uterine cancer: endometrial cancer and uterine sarcoma. Endometrial cancers arise in the lining of the uterus whereas uterine sarcomas develop in the muscle

2019 Cancer Australia

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