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ClinicalA 13-month-old male patient presented with disproportionate overgrowth of the left foot big toe (Figure 1). There was no family history and other anomalies were not detected.Plain radiography of the left foot revealed an enlarged distal phalanx of the big toe, together with thick soft tissue. To obtain a detailed view of the bone or soft tissue pathologies, computed tomography (CT) was performed using a 16-detector-row CT scanner (multidetector CT, Aquillon; Toshiba Medical Systems, Tokyo, Japan).CT scan revealed macrodactyly with hypertrophy of the subcutaneous fat tissue and enlargement of the bone in the big toe (Figure 2). Magnetic resonance imaging (MRI; 1,5 Tesla, Siemens, Germany) imaging showed in detail prominent proliferation of fatty tissue of the big toe (Figure 3). Figure 1. Clinical image shows overgrowth of the left foot big toe Figure 2. 3-D volume rendering image shows enlargement of the bone in the big toe. It shows dorsiflexion of big toe due to hypertrophy of the fat tissue Figure 3. T1-weighted axial image shows prominent proliferation of fatty tissue of the big toe DiscussionMacrodystrophia lipomatosa, termed congenital macrodactyly, is a rare congenital malformation characterised by progressive enlargement of all mesenchymal elements of the digit, except the metacarpal and metatarsal.1 It is more common on the hand than the foot. Soft tissue hypertrophy is most marked in the distribution of the plantar or median nerves.2 The differential diagnosis of macrodactyly includes acquired causes such as dactylitis secondary to infection, infarction and osteoid osteoma, Stills disease, melorheostosis, and congenital causes including haemangioma, lymphangioma, plexiform neurofibroma.3,4 In addition, fibrolipomatous hamartoma and fibrolipoma should be considered in different diagnosis.4 Multiplanar reconstruction and three-dimensional (3-D) volume rendering imaging features of multidetector CT and MR images give important information in different diagnosis of pathologies causing macrodactyly.

Summary

Abstract

Aim

Method

Results

Conclusion

Author Information

Mustafa Koplay1; Mecit Kantarci2; G 00f6kcen Kilinc2. 1. Department of Radiology, Selcuklu Medical Faculty, Selcuk University, Konya, Turkey. 2. Department of Radiology, Medical Faculty, Atat 00fcrk University, Erzurum, Turkey

Acknowledgements

Correspondence

Mustafa Koplay MD, Selcuk University, Selcuklu Medical Faculty, Department of Radiology, The Central Campus, 42075, Konya, Turkey.

Correspondence Email

koplaymustafa@hotmail.com

Competing Interests

Kotwal PP, Farooque M. Macrodactyly. J Bone Joint Surg Br 1998;80:651-3.D'Costa GF, Taksande RV, Pandya BS, et al. Macrodystrophia lipomatosa: a case report. Indian J Pathol Microbiol 2007;50:572-4.Goldman AB, Kaye JJ. Macrodystrophia lipomatosa: radiographic diagnosis. AJR Am J Roentgenol 1977;128:101-5.Krengel S, Fustes-Morales A, Carrasco D, et al. Macrodactyly: report of eight cases and review of the literature. Pediatr Dermatol 2000;17:270-6.

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ClinicalA 13-month-old male patient presented with disproportionate overgrowth of the left foot big toe (Figure 1). There was no family history and other anomalies were not detected.Plain radiography of the left foot revealed an enlarged distal phalanx of the big toe, together with thick soft tissue. To obtain a detailed view of the bone or soft tissue pathologies, computed tomography (CT) was performed using a 16-detector-row CT scanner (multidetector CT, Aquillon; Toshiba Medical Systems, Tokyo, Japan).CT scan revealed macrodactyly with hypertrophy of the subcutaneous fat tissue and enlargement of the bone in the big toe (Figure 2). Magnetic resonance imaging (MRI; 1,5 Tesla, Siemens, Germany) imaging showed in detail prominent proliferation of fatty tissue of the big toe (Figure 3). Figure 1. Clinical image shows overgrowth of the left foot big toe Figure 2. 3-D volume rendering image shows enlargement of the bone in the big toe. It shows dorsiflexion of big toe due to hypertrophy of the fat tissue Figure 3. T1-weighted axial image shows prominent proliferation of fatty tissue of the big toe DiscussionMacrodystrophia lipomatosa, termed congenital macrodactyly, is a rare congenital malformation characterised by progressive enlargement of all mesenchymal elements of the digit, except the metacarpal and metatarsal.1 It is more common on the hand than the foot. Soft tissue hypertrophy is most marked in the distribution of the plantar or median nerves.2 The differential diagnosis of macrodactyly includes acquired causes such as dactylitis secondary to infection, infarction and osteoid osteoma, Stills disease, melorheostosis, and congenital causes including haemangioma, lymphangioma, plexiform neurofibroma.3,4 In addition, fibrolipomatous hamartoma and fibrolipoma should be considered in different diagnosis.4 Multiplanar reconstruction and three-dimensional (3-D) volume rendering imaging features of multidetector CT and MR images give important information in different diagnosis of pathologies causing macrodactyly.

Summary

Abstract

Aim

Method

Results

Conclusion

Author Information

Mustafa Koplay1; Mecit Kantarci2; G 00f6kcen Kilinc2. 1. Department of Radiology, Selcuklu Medical Faculty, Selcuk University, Konya, Turkey. 2. Department of Radiology, Medical Faculty, Atat 00fcrk University, Erzurum, Turkey

Acknowledgements

Correspondence

Mustafa Koplay MD, Selcuk University, Selcuklu Medical Faculty, Department of Radiology, The Central Campus, 42075, Konya, Turkey.

Correspondence Email

koplaymustafa@hotmail.com

Competing Interests

Kotwal PP, Farooque M. Macrodactyly. J Bone Joint Surg Br 1998;80:651-3.D'Costa GF, Taksande RV, Pandya BS, et al. Macrodystrophia lipomatosa: a case report. Indian J Pathol Microbiol 2007;50:572-4.Goldman AB, Kaye JJ. Macrodystrophia lipomatosa: radiographic diagnosis. AJR Am J Roentgenol 1977;128:101-5.Krengel S, Fustes-Morales A, Carrasco D, et al. Macrodactyly: report of eight cases and review of the literature. Pediatr Dermatol 2000;17:270-6.

For the PDF of this article,
contact nzmj@nzma.org.nz

View Article PDF

ClinicalA 13-month-old male patient presented with disproportionate overgrowth of the left foot big toe (Figure 1). There was no family history and other anomalies were not detected.Plain radiography of the left foot revealed an enlarged distal phalanx of the big toe, together with thick soft tissue. To obtain a detailed view of the bone or soft tissue pathologies, computed tomography (CT) was performed using a 16-detector-row CT scanner (multidetector CT, Aquillon; Toshiba Medical Systems, Tokyo, Japan).CT scan revealed macrodactyly with hypertrophy of the subcutaneous fat tissue and enlargement of the bone in the big toe (Figure 2). Magnetic resonance imaging (MRI; 1,5 Tesla, Siemens, Germany) imaging showed in detail prominent proliferation of fatty tissue of the big toe (Figure 3). Figure 1. Clinical image shows overgrowth of the left foot big toe Figure 2. 3-D volume rendering image shows enlargement of the bone in the big toe. It shows dorsiflexion of big toe due to hypertrophy of the fat tissue Figure 3. T1-weighted axial image shows prominent proliferation of fatty tissue of the big toe DiscussionMacrodystrophia lipomatosa, termed congenital macrodactyly, is a rare congenital malformation characterised by progressive enlargement of all mesenchymal elements of the digit, except the metacarpal and metatarsal.1 It is more common on the hand than the foot. Soft tissue hypertrophy is most marked in the distribution of the plantar or median nerves.2 The differential diagnosis of macrodactyly includes acquired causes such as dactylitis secondary to infection, infarction and osteoid osteoma, Stills disease, melorheostosis, and congenital causes including haemangioma, lymphangioma, plexiform neurofibroma.3,4 In addition, fibrolipomatous hamartoma and fibrolipoma should be considered in different diagnosis.4 Multiplanar reconstruction and three-dimensional (3-D) volume rendering imaging features of multidetector CT and MR images give important information in different diagnosis of pathologies causing macrodactyly.

Summary

Abstract

Aim

Method

Results

Conclusion

Author Information

Mustafa Koplay1; Mecit Kantarci2; G 00f6kcen Kilinc2. 1. Department of Radiology, Selcuklu Medical Faculty, Selcuk University, Konya, Turkey. 2. Department of Radiology, Medical Faculty, Atat 00fcrk University, Erzurum, Turkey

Acknowledgements

Correspondence

Mustafa Koplay MD, Selcuk University, Selcuklu Medical Faculty, Department of Radiology, The Central Campus, 42075, Konya, Turkey.

Correspondence Email

koplaymustafa@hotmail.com

Competing Interests

Kotwal PP, Farooque M. Macrodactyly. J Bone Joint Surg Br 1998;80:651-3.D'Costa GF, Taksande RV, Pandya BS, et al. Macrodystrophia lipomatosa: a case report. Indian J Pathol Microbiol 2007;50:572-4.Goldman AB, Kaye JJ. Macrodystrophia lipomatosa: radiographic diagnosis. AJR Am J Roentgenol 1977;128:101-5.Krengel S, Fustes-Morales A, Carrasco D, et al. Macrodactyly: report of eight cases and review of the literature. Pediatr Dermatol 2000;17:270-6.

Contact diana@nzma.org.nz
for the PDF of this article

View Article PDF

ClinicalA 13-month-old male patient presented with disproportionate overgrowth of the left foot big toe (Figure 1). There was no family history and other anomalies were not detected.Plain radiography of the left foot revealed an enlarged distal phalanx of the big toe, together with thick soft tissue. To obtain a detailed view of the bone or soft tissue pathologies, computed tomography (CT) was performed using a 16-detector-row CT scanner (multidetector CT, Aquillon; Toshiba Medical Systems, Tokyo, Japan).CT scan revealed macrodactyly with hypertrophy of the subcutaneous fat tissue and enlargement of the bone in the big toe (Figure 2). Magnetic resonance imaging (MRI; 1,5 Tesla, Siemens, Germany) imaging showed in detail prominent proliferation of fatty tissue of the big toe (Figure 3). Figure 1. Clinical image shows overgrowth of the left foot big toe Figure 2. 3-D volume rendering image shows enlargement of the bone in the big toe. It shows dorsiflexion of big toe due to hypertrophy of the fat tissue Figure 3. T1-weighted axial image shows prominent proliferation of fatty tissue of the big toe DiscussionMacrodystrophia lipomatosa, termed congenital macrodactyly, is a rare congenital malformation characterised by progressive enlargement of all mesenchymal elements of the digit, except the metacarpal and metatarsal.1 It is more common on the hand than the foot. Soft tissue hypertrophy is most marked in the distribution of the plantar or median nerves.2 The differential diagnosis of macrodactyly includes acquired causes such as dactylitis secondary to infection, infarction and osteoid osteoma, Stills disease, melorheostosis, and congenital causes including haemangioma, lymphangioma, plexiform neurofibroma.3,4 In addition, fibrolipomatous hamartoma and fibrolipoma should be considered in different diagnosis.4 Multiplanar reconstruction and three-dimensional (3-D) volume rendering imaging features of multidetector CT and MR images give important information in different diagnosis of pathologies causing macrodactyly.

Summary

Abstract

Aim

Method

Results

Conclusion

Author Information

Mustafa Koplay1; Mecit Kantarci2; G 00f6kcen Kilinc2. 1. Department of Radiology, Selcuklu Medical Faculty, Selcuk University, Konya, Turkey. 2. Department of Radiology, Medical Faculty, Atat 00fcrk University, Erzurum, Turkey

Acknowledgements

Correspondence

Mustafa Koplay MD, Selcuk University, Selcuklu Medical Faculty, Department of Radiology, The Central Campus, 42075, Konya, Turkey.

Correspondence Email

koplaymustafa@hotmail.com

Competing Interests

Kotwal PP, Farooque M. Macrodactyly. J Bone Joint Surg Br 1998;80:651-3.D'Costa GF, Taksande RV, Pandya BS, et al. Macrodystrophia lipomatosa: a case report. Indian J Pathol Microbiol 2007;50:572-4.Goldman AB, Kaye JJ. Macrodystrophia lipomatosa: radiographic diagnosis. AJR Am J Roentgenol 1977;128:101-5.Krengel S, Fustes-Morales A, Carrasco D, et al. Macrodactyly: report of eight cases and review of the literature. Pediatr Dermatol 2000;17:270-6.

Contact diana@nzma.org.nz
for the PDF of this article

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