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Osteopoikilosis Radiology

OF the many obscure benign systemic bone diseases, osteopoikilosis (ostitis condensans generalisata or osteopathia condensans disseminata) is one of the most interesting. It is a congenital hereditary condition in which there are found small areas of compact bone within the cancellated structures of almost all the bones except the skull OSTEOPOIKILOSIS is a comparatively rare disorder which is generally conceded to be an anomaly of the skeletal structure that, because it is usually asymptomatic, is discovered most frequently by accident in the course of roentgenographic examination for evidence of, or for the cause of, other lesions Osteopoikilosis is an autosomal dominant sclerosing bone dysplasia that results in focal deposits of thickened lamellar bone in the spongiosa. 1 Albers-Schonberg and Ledoux-Lebard initially characterized osteopoikilosis in 1915 Incidentally noted multiple intraosseous lesions that are small in size, discrete and show low signal on T1WI and T2WI, mostly representing osteopoikilosis. Osteopoikilosis is characterized by multiple benign enostoses. It is usually incidentally found on skeletal x-rays. It is always asymptomatic Discussion Osteopoikilosis (osteopathia condensans disseminata) is a rare sclerosing bone dysplasia of unknown etiology. It is also known as Albers-Schonberg disease or by its Latin name, osteopathia condensans disseminata, which describes its main features

Osteopoikilosis Radiolog

Clear both lung fields and costophrenic angles. Linear fracture is seen in the posterior aspect of the left first rib. Multiple bones islands are seen in both proximal humerus and glenoids suggesting osteopoikilosis The above MRI studies show multiple ovoid, hypointense areas within the marrow cavity which are hypointense on all sequences, consistent with the appearance of multiple bone islands. They are juxta-articular in location and involving all extra-axial joints in a bilaterally symmetric fassion. These are diagnostic findings of osteopoikilosis Osteopoikilosis. Black arrows point to numerous sclerotic bone islands surrounding the hip joints in a pattern characteristic of osteopoikilosis. CT images of the same patient show the well-circumscribed lesions in the femurs and pelvis. For these same photos without the arrows, click here and her

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Osteopoikilosis I. Seth Hirsch , M.D. New York City Excerpt OF the many obscure benign systemic bone diseases, osteopoikilosis (ostitis condensans generalisata or osteopathia condensans disseminata) is one of the most interesting. It is a congenital hereditary condition in which there are found small areas of compact bone within the cancellated structures of almost all the bones except the. Osteopoikilosis. Osteopoikilosis is a disorder of endochondral ossification involving the secondary spongiosa. The bone lesions are asymptomatic, although there is a frequent association with dermatofibrosis lenticularis disseminata, a connective tissue disorder characterized by papular fibromas throughout the extremities and back. Osteopoikilosis is a benign condition first documented by the German surgeon Alfred Stieda in 1905 and attributed to Heinrich Ernst Albers-Schönberg, a German radiologist and surgeon who published it in 1915 [1,2,3,4]

Osteopoikilosis. Brian Edward Reeves, Anthony G. Ryan, Peter L. Munk, and Thomas Pope. Clinical Presentation. A 55-year-old man presented with right hip pain after a motor vehicle accident. An AP pelvic film and a preoperative chest x-ray were performed Case of the Week 415 on award-winning, radiologic teaching site for medical students and those starting out in radiology focusing on chest, GI, cardiac and musculoskeletal diseases containing over 200 PowerPoint lectures, quizzes, hand-out notes, interactive material, most commons lists and pictorial differential diagnose Osteopoikilosis is a condition in which many small, roundish spots are found in the bones, particularly near the joints. These spots are areas of bone tissue that did not develop properly and are exceptionally dense. They usually do not cause symptoms and do not change over time. Osteopoikilosis can be diagnosed at any age and is often detected by chance when an otherwise healthy individual.

Osteopoikilosis | Image | Radiopaedia

Article - Osteopoikilosis - Applied Radiolog

  1. ant fashion 1, 2.Although this form of dysplasia is asymptomatic and requires no treatment, in cases with coexisting various pathological condition and complications, medical attention was required 3, 4, 5.. Roentgenographic findings are diagnostic
  2. Anatomico-pathological and radiological studies of osteopoikilosis were performed in two cases, one involving a femoral head, excised after a fracture of a femoral neck, in an elderly man and the other following biopsy of an iliac crest in a young woman. In both patients wide-spread radiological evi
  3. Treatment for osteopoikilosis in Mumbai, find doctors near you. Book Appointment Online, View Fees, Reviews Doctors for Osteopoikilosis Radiology in Mumbai | Pract
  4. Osteopoikilosis | Radiology Case | Radiopaedia.org. Incidental finding of Osteopoikilosis which is a sclerosing bony dysplasia with multiple enostoses. Radiopaedia. 17k followers. Technology World. Medical Technology. Science And Technology. Technology Innovations. Technology Careers. Hand Surgery
  5. Technetium-99m pyrophosphate bone images were contrasted with radiographic findings in two patients with osteopoikilosis, one with osteopathia striata, and one with melorheostosis. Despite the striking radiographic findings, scans were normal in osteopoikilosis and osteopathia striata

Treatment for osteopoikilosis in Gurgaon, find doctors near you. Book Appointment Online, View Fees, Reviews Doctors for Osteopoikilosis Radiology in Gurgaon | Pract Osteopoikilosis is a rare bone disorder diagnosed at imaging. Because of its characteristic imaging appearance, it is considered a skeletal don't touch lesion. In certain patients with a known osteoblastic tumor, it may be difficult to differentiate osteopoikilosis from osteoblastic metastasis Osteopoikilosis (osteopathia condensans disseminata, spotted bones) was first described by Stieda (1905) and subsequently by Albers-Schönberg and Ledoux-Lebard. It is a rare abnormality in the enchondral bone maturation process; generally transmitted in an autosomal dominant fashion in a which osteosclerotic dysplasia of bone develops during. Osteopoikilosis, osteopathia condensans disseminata, osteopoecilia, osteosclerosis fragilis generalisata, or Albers-Schönberg disease, is a pathologic condition of the skeleton characterized by the presence of multiple, small, widely disseminated areas of compact bone. It is probably a congenital anomaly of hereditary background

Osteopoikilosis represents an autosomal dominant bone dysplasia that mimics osteoblastic bone metastases, and may lead to misdiagnosis and unnecessary treatment. Its incidence is 1 in 50, 000; it is seen in up to 6 per 100, 000 radiographs. [1] A mutation in gene LEMD3 at position 12q13 is responsible for this benign bone condition Radiology Case. 2009 Dec; 3(12):38-43 :: DOI: 10.3941/jrcr.v3i12.260 ABSTRACT Osteopoikilosis (OP) is a very rare benign sclerosing bony dysplasia with an autosomal dominant inheritance. We describe the morphology of an osteopoikilosis male patient, associated with severe pain on wrist and han Anatomico-pathological and radiological studies of osteopoikilosis were performed in two cases, one involving a femoral head, excised after a fracture of a femoral neck, in an elderly man and the other following biopsy of an iliac crest in a young woman. In both patients wide-spread radiological evidence of the disorder was present as an incidental finding HUG (Hospital Universitary Geneva), Department of Radiology, Geneva, Switzerland. Osteopoïkilosis Close. 1 x. PA view of the left hand. Numerous well defined small circular opacities located in the peri-articular regions of the bones of the wrist and the metacarpophalangeal joints Receive the radRounds Radiology Newsletter featuring breaking news, educational resources, and latest job opportunities. New subscribers randomly selected for free $25 Starbucks Gift Card (*One recipient per week limit

Osteopoikilosis Radiology Case Radiopaedia

  1. ant hereditary pattern [1-3]. It has an estimated reported incidence of 1:50,000 with a male to female ratio of 3:2 [4]. The genetic predisposition to this condition has been linked to a heterozygous mutation of the LEMD3 gene [5]
  2. Osteopoikilosis should be considered in the differential diagnosis of multiple osteosclerotic bone lesions, but is a relatively uncommon finding. Serowy (1956) could find only 100 reported cases in the literature over a 25-year period since its initial description, and Jonasch (1955) found only 12 cases of osteopoikilosis in a series of 21000.
  3. OSTEOPOIKILOSIS: AN INCIDENTAL FINDING IN A PATIENT WITH OLECRANON FRACTURE PAKISTAN JOURNAL OF RADIOLOGY PJR April - June 2012; 22(2) 59 Yasir Jameel Khatak, Tariq Alam, Zafar Sajjad Correspondence : Dr. Yasir Jameel Khatak Department of Radiology, The Aga Khan University Hospital, Karachi - Pakistan. Tel No.: 34930051 - Ext. 202
  4. Abstract. Anatomico-pathological and radiological studies of osteopoikilosis were performed in two cases, one involving a femoral head, excised after a fracture of a femoral neck, in an elderly man and the other following biopsy of an iliac crest in a young woman. In both patients wide-spread radiological evidence of the disorder was present as.
  5. ant fashion [].Its incidence is estimated to be one in every 50,000 individuals [2, 3].On radiographs, it is characterized by multiple sclerotic foci that correspond to condensations of the lamellar trabeculae on histology []
  6. Osteopoikilosis: A radiological and pathological study Osteopoikilosis: A radiological and pathological study Lagier, R.; Mbakop, A.; Bigler, A. 1984-03-01 00:00:00 256 11 11 3 3 R. Lagier M.D. A. Mbakop M.D. A. Bigler M.D. Department of Pathology, Osteoarticular Unit Geneva Medical School Geneva Switzerland Department of Surgery, Orthopaedic Clinic Geneva Medical School Geneva Switzerland.
  7. Treatment for osteopoikilosis in Thane, find doctors near you. Book Appointment Online, View Fees, Reviews Doctors for Osteopoikilosis Radiology in Thane | Pract

Article - Osteopoikilosis (OPK) - Applied Radiolog

1. Can Fam Physician. 1999 Oct;45:2315, 2318-20. Radiology rounds. Osteopoikilosis. McLennan MK(1). Author information: (1)Markham Stouffville Hospital, Ont. PMCID. Radiology case of the month. Left shoulder pain following trauma. Osteopoikilosis. Flynt K, Johnston S, Neitzschman HR. J La State Med Soc, 162(6):315-316, 01 Nov 2010 Cited by: 0 articles | PMID: 2129448 Radiology 1935; 25:349-354 [Google Scholar] 17. Paraskevas G, Raikos A, Stavrakas M, Spanidou S, Papaziogas B. Osteopoikilosis: a case report of a symptomatic patient

Osteopoikilosis - on MRI Radiology Case Radiopaedia

LearningRadiology - Osteopoikilosis, Spotted, Bone

Osteopoikilosis is a rare disease; the incidence of 1/50,000 reported by other authors was borne out by the findings of the present study—ten cases in a catchment population of roughly 500,000. However, the real incidence may actually be higher: osteopoikilosis is a hereditary condition, generally transmitted as an autosomal dominant trait. Osteopoikilosis is a rare bone dysplasia. Patients are generally asymptomatic and are frequently identified during radiological imaging by coincidence Anteroposterior, right hand radiograph. Multiple radio-opaque circular or ovoid dense spots with define linear sclerotic circumference, located at the proximal and distal epiphyses of (here 4 th and 5 th ) phalanges and metacarpals are noticed.Figure 1 (1magnified viewcomplete hand radiograph on next page): 50-year-old man with osteopoikilosis Osteopoikilosis Shuzhong Liu 1 , Xi Zhou 2 , An Song 3 , Zhen Huo 4 , Yong Liu 5 , Yipeng Wang 6 Radiology and morphology of spotted bone: a case report with review of literature. Bidarkotimath S, Murlimanju BV, Dhananjaya KV..

Osteopoikilosis: Report of Two Cases Radiolog

ABSTRACT: Osteopoikilosis is a rare, benign osteosclerotic dysplasia that predominantly involves the appendicular skeleton. Radiographic findings are diagnostic, and the disease often is discovered incidentally on x-ray films. The importance of recognizing osteopoikilosis lies in differentiating it from osteoblastic metastases. The cause is unclear 1. Radiology. 1978 May;127(2):439-43. 99mTc-pyrophosphate bone imaging in osteopoikilosis, osteopathia striata, and melorheostosis. Whyte MP, Murphy WA, Siegel BA. Technetium-99m pyrophosphate bone images were contrasted with radiographic findings in two patients with osteopoikilosis, one with osteopathia striata, and one with melorheostosis

Osteopoikilosis (OPK) is a benign, rare, asymptomatic osteosclerotic bone dysplasia which is inherited as an autosomal dominant trait. It may develop during childhood and persists throughout life Author information: (1)Department of Radiology and Pathology, North General Hospital 10035. An unusual case of osteopoikilosis was found in a 52-year-old black woman. The rather large diffuse focal increased densities involving the ribs, spine, and pelvis as seen in the roentgenograms were believed to represent metastatic bone lesions 3 Radiology, Hospital Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain. PMID: 30951020 DOI: 10.1097/MPH.0000000000001457 Abstract Osteopoikilosis (OPK) is a rare, benign, asymptomatic bone disease causing dense bone lesions, which could be interpreted as bone metastasis. The symmetric distribution, lack of bone destruction, and. The patient was informed of the unusual findings, and the need for a specialist opinion to make the correct diagnosis. After discussion with the radiology department, further x rays were taken of his pelvis and contralateral ankle, both of which demonstrated a similar appearance. The diagnosis of osteopoikilosis was confirmed after a week

Osteopoikilosis - Sumer's Radiology Blo

Progression of osteopoikilosis Eurora

Differentiating osteopoikilosis from osteoblastic metastase

Osteopoikilosis - an overview ScienceDirect Topic

  1. Osteopoikilosis is a rare bone anomaly usually benign which may be confused with other severe primary diseases or dangerous metastatic bone lesions. Standard radiology, computed tomography (CT.
  2. Osteopoikilosis was first described by Albers-Schonberg in 1915. It is a benign, usually asymptomatic condition diagnosed radiographically by the presence of multiple symmetrical circular/ovoid sclerotic opacities of the ischia, pubic bones, and the epimetaphysial regions of the short tubular bones
  3. Osteopoikilosis. This disorder is considered to be very common. It is characterized by small round or oval foci of bone sclerosis located in the trabecular bone, particularly in the pelvis, metaphyses and epiphyses of long bones, tarsals, and carpals. Radiology of Syndromes, Metabolic Disorders, and Skeletal Dysplasias. Besides providing a.
  4. LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis. Calcif Tissue Int 81:81-84 10. Seron MA, Yochum TR (1996) Essentials of skeletal radiology. Williams & Wilkins, Baltimore, pp 630-633 11. Appenzeller S, Castro GR, Coimbra IB (2007) Osteopoikilosis with abnormal bone scan: long-term follow-up. J Clin.
  5. Osteopoikilosis or 'spotted bones' is a benign condition in which multiple sclerotic foci are associated with patches of lentil-like papules in the skin. Stieda (1905) is credited with the first description of osteopoikilosis, and Ledoux-Lebard et al. (1916) subsequently coined the term osteopoecilie from the Greek word poikilos , meaning.
  6. Osteopoikilosis. 16. CT scan of pelvis in a patient with osteopoikilosis. 17. AP plain film radiograph and coronal section MR sequence of the left elbow showing osteopoikilosis. 18. Osteopoikilosis MRI of the ankle for research of a posterior impingement. 19. Osteopoikilosis - MRI features. 20

Osteopoikilosis, Radiology 10

Osteopoikilosis is an asymptomatic osteosclerotic dysplasia initially described by Albers Schönberg in 1915. Osteopoikilosis is a rare disease with an estimated incidence of 1/50,000 and with an. Radiology 127:439-443 losis. Orthop Clin 166:89-92 21. Tong ECK, Samii M, Tchang F (1988) Bone imaging as an aid 14. Sarralde A, Garcı´ a-Cruz D, Nazara A, Sa´nchez-Corona J for the diagnosis of osteopoikilosis Ependymomas are benign neoplasms effecting the spinal cord seen usually in the third to sixth decade. They grow longitudinally over several vertebral segments and eventually produce erosion of vertebral components. They enhance diffusely. Symptoms include back pain and radiculopathies of the lower extremities. lateral radiograph and ct images. It may coexist in a so-called overlap syndrome known as mixed sclerosing bone dystrophy (MSBD) with osteopoikilosis and osteopathia striata, as well as with tumors, vascular malformations, lymphangiectasis, or fibrolipomatous lesions. Typically, the cutaneous and other clinical features occur in the same sclerotome as the affected bone(s). Etiolog osteopoikilosis: [ os″te-o-poi″kĭ-lo´sis ] a mottled condition of bones, apparent radiographically, due to the presence of multiple sclerotic foci and scattered stippling. adj., adj osteopoikilot´ic

Sclerosing Bone Dysplasias: Review and Differentiation

diameter consistent with osteopoikilosis were noted around in the wrists, fingers and metacarps and evaluated as compatible with osteopoikilosis (Figure 1). Considering that osteopoikilosis can be seen in various bones, PA lung radiography, pelvic radiograph, knee and ankle radiographs were obtained by including shoulder joints A 17-year-old boy came to our hospital with a wound infection 5 days after urological surgery. CT scan done to assess the depth of the infection showed multiple well circumscribed, ovoid, radiodense bony lesions in the pelvis and proximal femurs, consistent with the diagnosis of osteopoikilosis. Osteopoikilosis or spotted bone disease is a rare, benign, autosomal dominant disorder. Case report: osteopoikilosis and the Buschke-Ollendorff syndrome The British Journal of Radiology , 66 ( 1993 ) , pp. 468 - 470 CrossRef View Record in Scopus Google Schola When considering congenital causes of sclerotic lesions, benign causes such as bone islands or osteopoikilosis usually have a fairly typical appearance and are hard to mistake. Osteopetrosis and pyknodysostosis are likewise hard to mistake for other entities since the bones are denser than in any other disorder, and the long bones tend to have. To the Editor.— The letter Otosclerosis Associated With Osteopoikilosis (1981;246:2030) raises some interesting points. In 1967, 1 I published two reports of cases of familial juvenile elastoma with otosclerosis and osteopoikilosis and commented that although the presence of otosclerosis in case 1 may have been fortuitous, it was possible that a bony plaque similar to those found in the.

To the Editor.— Osteopoikilosis is a rare bone dysplasia thought to be inherited by an autosomal dominant mechanism. 1 It is characterized by. numerous spheroid nodules in the spongiosa of the metaphysis and epiphysis. The bones involved most often are the long bones and the small bones of the hands, feet, and pelvis. Osteopoikilosis usually is found incidentally on roentgenography Osteopoikilosis. Osteopoikilosis, also called spotted bone disease, is a rare, benign, autosomal dominant disorder. The pathognomonic appearance includes sclerotic bone lesions most commonly involving the hands, feet, pelvis, and ends of long bones in a symmetric distribution, especially around the joints Osteopoikilosis (OPK) or spotted bones is a sclerosing bone dysplasia caused by a resorption failure of secondary spongy bone (Woyciechowsky et al., 2012). As the word suggests, this condition consists of multiple sclerotic foci that are observed as radiodense areas (Resnick and Kransdorf, 2005:1425)

CHORUS is a hypertext medical reference. More than 1100 documents describe diseases, anatomy, and radiologic findings [Osteopoikilosis.] WANG ST. Zhonghua Fang she xue za zhi Chinese Journal of Radiology, 01 Feb 1960, 8: 56-57 Language: chi PMID: 13842810 . Share this article Share with email Share with twitter Share with linkedin Share with facebook. Abstract . No abstract provided. Similar Articles.

Rationale: Osteopoikilosis is a rare and asymptomatic disease of the bone, which is often discovered occasionally on radiography for irrelevant complaints. Characterized by multiple, small, circular, or oval-shaped radiodense lesions, it may be confused with bony metastatic tumors. Patient concerns: The present study describes a case of a 17-year-old adolescent who suffered from pain and. Dec 24, 2019 - Explore Abdulrhman Ahmed's board عبوود on Pinterest. See more ideas about radiology imaging, radiology, radiography Osteopoikilosis (OPK) is a rare inherited condition of the bones, transmitted as an autosomal dominant trait characterized by numerous hyperostotic areas that tend to localize in periarticular osseous regions. It is usually asymptomatic and is often diagnosed incidentally during x-rays made by other reasons Osteopoikilosis, multiple bone islands, is a condition of unknown origin which is transmitted in an autosomal dominant manner. The multiple, sclerotic, roundish lesions vary in size from a few millimeters to several centimeters. They are scattered within the cancellous bone and concentrated near the joint surfaces Chapter 100 covers osteopoikilosis (MIM 166700), including major clinical findings, radiographic features, and differential diagnoses. Access to the complete content on Oxford Medicine Online requires a subscription or purchase

Osteopoikilosis presents as round or ovoid sclerotic lesions with an appearance like enostosis on pathology. Synovial osteochondromatosis occurs due to cartilaginous metaplasia with synovial villous proliferation with calcified nodules in proximity to joints. A case of osteopoikilosis associated with synovial osteochondromatosis is described It was suggested that the [6] G. Paraskevas, A. Raikos, M. Stavrakas, S. Spanidou, and B. deinitive diagnosis of OPK could be made by radiography of Papaziogas, Osteopoikilosis: a case report of a symptomatic 4 Case Reports in Orthopedics patient, Journal of Radiology Case Reports, vol. 3, no. 12, pp. 38- 43, 2009. [7 Osteopoikilosis (OPK) is a benign rare disorder of the endochondral bone, characterized by small multiple osteocondensation lesions, maximum 10 mm, usually found in the long bones of the limbs, hand, foot, pelvis and spine. These findings are suggestive of osteopoikilosis. Similar lesions were also present in the contralateral hand and wrist.

Osteopoikilosis (OPK) is a benign rare disorder of the endochondral bone, characterized by small multiple osteocondensation lesions, maximum 10 mm, usually found in the long bones of the limbs, hand, foot, pelvis and spine. The lesions are symmetrically distributed. Often, the diagnosis is made by chance, like in our case. Case Repor Metastatic bone disease describes a malignant tumor that secondarily seeds to bone, usually from a primary malignancy of the epithelial tissue (designated as carcinomas) of the lung, breast, prostate, kidney, liver, and so on.For instance, if the patient has a bronchogenic carcinoma that metastasizes to the thoracic spine, the lung lesion is the primary lesion and the thoracic spine lesion is. Isolated melorheostosis without osteopoikilosis is also generally a sporadic condition, but osteopoikilosis has been described as an autosomal‐dominant trait. The finding of mixed sclerosing bone dysplasia in a family with osteopoikilosis suggests that the melorheostotic component of this disorder may be due to a second mutation at the same.

The histological appear- ance of a bone island is, in fact, the same as that seen in osteopoikilosis. The radiological features of the two conditions are also similar except that the former is usually solitary, whereas the latter consists of multiple areas of sclerosis. There is a strong hereditary tendency in osteopoikilosis There is a wide variety of hereditary and non-hereditary bone dysplasias, many with unique radiographic findings. Hereditary bony dysplasias include osteopoikilosis, osteopathia striata, osteopetrosis, progressive diaphyseal dysplasia, hereditary multiple diaphyseal sclerosis and pyknodysostosis

Osteopoikilosis (OPK) is a rare benign sclerosing bone dysplasia and is often incidentally found on plain radiography. OPK generally does not require treatment. Nevertheless, osteonecrosis or degenerative joint disease can occur in the setting of OPK, and little is known with regard to the longevity of arthroplasty prostheses implanted into OPK-bearing bones Osteopoikilosis Normal bone scan in a person with osteopoikilosis List of radiographic Osteopoikilosis is a benign, autosomal dominant sclerosing dysplasia of bone characterized by the presence of numerous bone The radiographic appearance of osteopoikilosis on an X-ray is characterized by a pattern of numerous white densities of similar. N M Roberts, J A A Langtry, A C Branfoot, J Gleeson, R C D Staughton, Osteopoikilosis and the Buschke-Ollendorff syndrome, The British Journal of Radiology, 10.1259/0007-1285-66-785-468, 66, 785, (468-470), (1993) Osteopoikilosis is a rare autosomal dominant genetic disorder, characterised by the occurrence of the hyperostotic spots preferentially localized in the epiphyses and metaphyses of the long bones, and in the carpal and tarsal bones [1]. Heterozygous LEMD3 gene mutations were shown to be the primary cause of the disease [2]. Association of the primarily asymptomatic osteopokilosis with.

A rare benign disorder mimicking metastasis onOsteopoikilosis | Radiology Reference ArticleBone Island or Enostosis | Bone and Spine11 | Radiology KeySkeletal Radiology - Radiology 1 with Snedic at RANZCRBarton fracture | Radiology Case | RadiopaediaOsteopoikilosis | Eurorad

I would suggest osteopoikilosis however since it is an asymptomatic condition, I suspect one of the sclerotic foci could represent soft tissue calcification of rotator cuff tendons. A lateral shoulder radiograph and if needed shoulder ultrasound could further shed light on the condition Osteopoikilosis is a rare disease of the bone that is occasionally associated with skin lesions. The latter have been reported as dermatofibrosis lenticularis disseminata, juvenile elastoma, and connective-tissue nevus. The occurrence of this syndrome in three members of a family is used to.. osteopoikilosis: Collaborative Hypertext of Radiology [home, info] osteopoikilosis: Medical dictionary [home, info] Words similar to osteopoikilosis Usage examples for osteopoikilosis Words that often appear near osteopoikilosis Rhymes of osteopoikilosis